Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
UNKNOWN
Clinical Phase
PHASE2/PHASE3
Study Classification
INTERVENTIONAL
Study Start Date
2010-09-30
Brief Summary
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Several factors will be tested to see if they have an influence on the methacetin breath test results. Each one of the factors has been raised as a possible source of distortion of the MBT result.
I. Variability between same tests on same subject MBT. Repeatability will be tested in both healthy individuals and patients with chronic liver disease.
II. COPD - Chronic obstructive pulmonary disease is a leading cause of death worldwide, and can potentially have an effect on the MBT since the breath test is based on CO2 production and these subjects may have abnormal CO2 production.
III. Smoking- 13C Methacetin is metabolized by healthy hepatocytes reflecting hepatic microsomal function of CYP1A2, and smoking may cause induction of CYP1A2. Furthermore, internal preliminary data has shown signs that there is an influence of smoking on the MBT ranges.
IV. Age- Empirical data on several hundred subjects with chronic liver disease has shown that age is a significant factor in determining the probability of disease severity and preliminary data in normal subjects have shown changes in MBT with age.. Therefore, the effect of age has to be elucidated in an orderly fashion.
V. CYP450 1A2 Inhibitors- Several drugs and food items inhibit CYP450 1A2 and may affect the MBT.
VI. Alcohol - Alcohol ingestion leads to induction of hepatic CYP and at a later stage to inhibition due to liver damage. Acute alcohol ingestion may therefore effect MBT results.
VII. Beta-blockers - beta blocker are affecting portal hypertension and may affect hepatic blood flow and thereby the outcome of the methacetin breath test.
I. Variability between same tests on same subject MBT. Repeatability will be tested in both healthy individuals and patients with chronic liver disease.
II. COPD - Chronic obstructive pulmonary disease is a leading cause of death worldwide, and can potentially have an effect on the MBT since the breath test is based on CO2 production and these subjects may have abnormal CO2 production.
III. Smoking- 13C Methacetin is metabolized by healthy hepatocytes reflecting hepatic microsomal function of CYP1A2, and smoking may cause induction of CYP1A2. Furthermore, internal preliminary data has shown signs that there is an influence of smoking on the MBT ranges.
IV. Age- Empirical data on several hundred subjects with chronic liver disease has shown that age is a significant factor in determining the probability of disease severity and preliminary data in normal subjects have shown changes in MBT with age.. Therefore, the effect of age has to be elucidated in an orderly fashion.
V. CYP450 1A2 Inhibitors- Several drugs and food items inhibit CYP450 1A2 and may affect the MBT.
VI. Alcohol - Alcohol ingestion leads to induction of hepatic CYP and at a later stage to inhibition due to liver damage. Acute alcohol ingestion may therefore effect MBT results.
VII. Beta-blockers - beta blocker are affecting portal hypertension and may affect hepatic blood flow and thereby the outcome of the methacetin breath test.
Detailed Description
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Conditions
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Healthy Subjects
Chronic Liver Disease
Cirrhosis
Keywords
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Patients with chronic liver disease and cirrhosis
Study Groups
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Repeatability
Group Type
EXPERIMENTAL
13C Methacetin Breath Test
Intervention Type
DEVICE
COPD
Group Type
EXPERIMENTAL
13C Methacetin Breath Test
Intervention Type
DEVICE
Smokers
Group Type
EXPERIMENTAL
13C Methacetin Breath Test
Intervention Type
DEVICE
CYP450 1A2 Inhibitors
Group Type
EXPERIMENTAL
13C Methacetin Breath Test
Intervention Type
DEVICE
Grape fruit juice
Intervention Type
DIETARY_SUPPLEMENT
Cirrhosis Beta Blockers
Group Type
EXPERIMENTAL
13C Methacetin Breath Test
Intervention Type
DEVICE
Non selective beta blocker - Propranolol
Intervention Type
DRUG
Alcohol
Group Type
EXPERIMENTAL
13C Methacetin Breath Test
Intervention Type
DEVICE
Ethanol
Intervention Type
DIETARY_SUPPLEMENT
Interventions
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13C Methacetin Breath Test
Intervention Type
DEVICE
Grape fruit juice
Intervention Type
DIETARY_SUPPLEMENT
Non selective beta blocker - Propranolol
Intervention Type
DRUG
Ethanol
Intervention Type
DIETARY_SUPPLEMENT
Eligibility Criteria
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Inclusion Criteria
* Adult subjects with 18 years of age or older
* Women of childbearing potential must have a negative serum or urinary hCG pregnancy test within 7 days prior to enrollment. During the study these women must use 2 methods of contraception.
* Subject has given written informed consent, prior to any study related procedure not part of the subject's normal medical care, with the understanding that consent may be withdrawn at any time without prejudice to future medical care.
Healthy Subjects:
* No known liver disease
* Non smokers
* BMI =20-25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Not taking any medications
* No known on-going chronic medical conditions (apart from allergy or orthopaedic conditions not requiring chronic therapy).
* Normal abdominal ultrasound (US)
Cirrhotics:
* Diagnosis of cirrhosis by liver biopsy
* Or strong suspicion of cirrhosis by accepted criteria for the clinical diagnosis of cirrhosis (e.g. peripheral edema or varices, palpable hard left lobe of the liver, small right lobe span or palpable splenomegaly), and/or radiological evidence of cirrhosis (by abdominal sonography, computer assisted axial tomography, or magnetic resonance imaging, showing a nodular liver and/or portosystemic collaterals with portal vein patency and/or ascites and/or splenomegaly, and/or colloid shift on a colloid-isotope liver-spleen scan), and/or laboratory variables (platelets \<100,000/mm3, albumin\< 3.5g/dL, or INR \>1.3)
Chronic Liver Patient (non cirrhotic):
Patient who has been diagnosed with chronic liver disease for more than 6 months.
* No known liver disease
* BMI 20- 25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Patients with a COPD exacerbation with elevated PCO2 levels (\> 50 mmHg)
* Without clinically overt right heart failure
* Ceased smoking for at least one month
* No other overt clinical dysfunction of major organ system
Smokers:
* No known liver disease
* Active smoker of at least 10 cigarettes/day (stable number of cigarettes during past month - not currently trying to quit).
* BMI 20- 25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Not taking any medications
* No known chronic medical conditions
Healthy Subjects:
* No known liver disease
* Non smokers
* BMI 20- 25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Not taking any medications
* No known chronic medical conditions (allergy or orthopaedic condition not requiring chronic therapy allowed).
* Normal abdominal US
Cirrhotic subjects:
* Diagnosis of cirrhosis by liver biopsy
* Or strong suspicion of cirrhosis by accepted criteria for the clinical diagnosis of cirrhosis (e.g. peripheral edema or varices, palpable hard left lobe of the liver, small right lobe span or palpable splenomegaly), and/or radiological evidence of cirrhosis (by abdominal sonography, computer assisted axial tomography, or magnetic resonance imaging, showing a nodular liver and/or portosystemic collaterals with portal vein patency and/or ascites and/or splenomegaly, and/or colloid shift on a colloid-isotope liver-spleen scan), and/or laboratory variables (platelets \<100,000/mm3, albumin\< 3.5g/dL, or INR \>1.3)
* Not receiving medication which is metabolized by CYP450 1A2
* Diagnosis of cirrhosis (by liver biopsy or clinical diagnosis):
Strong suspicion of cirrhosis by accepted criteria for the clinical diagnosis of cirrhosis (e.g. peripheral edema or varices, palpable hard left lobe of the liver, small right lobe span or palpable splenomegaly), and/or radiological evidence of cirrhosis (by abdominal sonography, computer assisted axial tomography, or magnetic resonance imaging, showing a nodular liver and/or portosystemic collaterals with portal vein patency and/or ascites and/or splenomegaly, and/or colloid shift on a colloid-isotope liver-spleen scan), and/or laboratory variables (platelets \<100,000/mm3, albumin\< 3.5g/dL, or INR \>1.3)
* Naive to Beta Blockers - with a clinical indication for initiating therapy (eg. esophageal varices, portal hypertensive gastropathy)
* Resting pulse \> 60 beats per minute
* Non smoker
* No known liver disease
* Non smokers
* BMI 20- 25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Not taking any medications
* No known chronic medical conditions. (Allergy or orthopaedic condition not requiring chronic therapy allowed).
* Normal abdominal US
* Women of childbearing potential must have a negative serum or urinary hCG pregnancy test within 7 days prior to enrollment. During the study these women must use 2 methods of contraception.
* Subject has given written informed consent, prior to any study related procedure not part of the subject's normal medical care, with the understanding that consent may be withdrawn at any time without prejudice to future medical care.
Healthy Subjects:
* No known liver disease
* Non smokers
* BMI =20-25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Not taking any medications
* No known on-going chronic medical conditions (apart from allergy or orthopaedic conditions not requiring chronic therapy).
* Normal abdominal ultrasound (US)
Cirrhotics:
* Diagnosis of cirrhosis by liver biopsy
* Or strong suspicion of cirrhosis by accepted criteria for the clinical diagnosis of cirrhosis (e.g. peripheral edema or varices, palpable hard left lobe of the liver, small right lobe span or palpable splenomegaly), and/or radiological evidence of cirrhosis (by abdominal sonography, computer assisted axial tomography, or magnetic resonance imaging, showing a nodular liver and/or portosystemic collaterals with portal vein patency and/or ascites and/or splenomegaly, and/or colloid shift on a colloid-isotope liver-spleen scan), and/or laboratory variables (platelets \<100,000/mm3, albumin\< 3.5g/dL, or INR \>1.3)
Chronic Liver Patient (non cirrhotic):
Patient who has been diagnosed with chronic liver disease for more than 6 months.
* No known liver disease
* BMI 20- 25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Patients with a COPD exacerbation with elevated PCO2 levels (\> 50 mmHg)
* Without clinically overt right heart failure
* Ceased smoking for at least one month
* No other overt clinical dysfunction of major organ system
Smokers:
* No known liver disease
* Active smoker of at least 10 cigarettes/day (stable number of cigarettes during past month - not currently trying to quit).
* BMI 20- 25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Not taking any medications
* No known chronic medical conditions
Healthy Subjects:
* No known liver disease
* Non smokers
* BMI 20- 25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Not taking any medications
* No known chronic medical conditions (allergy or orthopaedic condition not requiring chronic therapy allowed).
* Normal abdominal US
Cirrhotic subjects:
* Diagnosis of cirrhosis by liver biopsy
* Or strong suspicion of cirrhosis by accepted criteria for the clinical diagnosis of cirrhosis (e.g. peripheral edema or varices, palpable hard left lobe of the liver, small right lobe span or palpable splenomegaly), and/or radiological evidence of cirrhosis (by abdominal sonography, computer assisted axial tomography, or magnetic resonance imaging, showing a nodular liver and/or portosystemic collaterals with portal vein patency and/or ascites and/or splenomegaly, and/or colloid shift on a colloid-isotope liver-spleen scan), and/or laboratory variables (platelets \<100,000/mm3, albumin\< 3.5g/dL, or INR \>1.3)
* Not receiving medication which is metabolized by CYP450 1A2
* Diagnosis of cirrhosis (by liver biopsy or clinical diagnosis):
Strong suspicion of cirrhosis by accepted criteria for the clinical diagnosis of cirrhosis (e.g. peripheral edema or varices, palpable hard left lobe of the liver, small right lobe span or palpable splenomegaly), and/or radiological evidence of cirrhosis (by abdominal sonography, computer assisted axial tomography, or magnetic resonance imaging, showing a nodular liver and/or portosystemic collaterals with portal vein patency and/or ascites and/or splenomegaly, and/or colloid shift on a colloid-isotope liver-spleen scan), and/or laboratory variables (platelets \<100,000/mm3, albumin\< 3.5g/dL, or INR \>1.3)
* Naive to Beta Blockers - with a clinical indication for initiating therapy (eg. esophageal varices, portal hypertensive gastropathy)
* Resting pulse \> 60 beats per minute
* Non smoker
* No known liver disease
* Non smokers
* BMI 20- 25 kg/m2
* Normal liver enzymes (ALT \< 40 U/L for men, \< 30 U/L for women)
* Not taking any medications
* No known chronic medical conditions. (Allergy or orthopaedic condition not requiring chronic therapy allowed).
* Normal abdominal US
Exclusion Criteria
* Severe heart, pulmonary or renal disease.
* Patient has previous surgical bypass surgery for morbid obesity
* Patient has extensive small bowel resection
* Any major surgery in the past 3 months.
* Patient is a recipient of any organ transplant
* Pregnant or breastfeeding women.
* Patient allergic to acetaminophen
* Patients who are taking hepatotoxic drugs
* Patient, based on the opinion of the investigator, should not be enrolled into this study.
* Patients unable or unwilling to sign informed consent
* Patients that are participating in other clinical trials evaluating experimental treatments or procedures or have participated in a clinical trial in the past 3 months.
* Patient has not fasted for 8 hours.
* Patient has smoked on the day of the test.
* Patient that has taken drugs that can interfere with methacetin metabolism: fluvoxamine, amiodarone, ciprofloxacin, cimetidine, rifampin, carbamazepine within the last 24 hours.
* Patient has taken Tylenol or any other acetaminophen related medications within the past 24 hours.
* Patients that received any new medication in the last 48 hours.
* Patients that still suffer from any previous clinical intervention (e.g. biopsy)
* Have not consumed alcohol 24 hours prior the MBT and not consume on a regular basis more than 40gr for male and 20gr for female per day.
General
* Severe heart, pulmonary or renal disease.
* Patient has previous surgical bypass surgery for morbid obesity
* Patient has extensive small bowel resection
* Any major surgery in the past 3 months.
* Patient is a recipient of any organ transplant
* Pregnant or breastfeeding women.
* Patient allergic to acetaminophen
* Patients who are taking hepatotoxic drugs
* Patient, based on the opinion of the investigator, should not be enrolled into this study.
* Patients unable or unwilling to sign informed consent
* Patients that are participating in other clinical trials evaluating experimental treatments or procedures or have participated in a clinical trial in the past 3 months.
* Patient has not fasted for 8 hours.
* Patient has smoked on the day of the test.
* Patient that has taken drugs that can interfere with methacetin metabolism: fluvoxamine, amiodarone, ciprofloxacin, cimetidine, rifampin, carbamazepine within the last 24 hours.
* Patient has taken Tylenol or any other acetaminophen related medications within the past 24 hours.
* Patients that received any new medication in the last 48 hours.
* Patients that still suffer from any previous clinical intervention (e.g. -
* Have not consumed alcohol 24 hours prior the MBT and not consume on a regular basis more than 40gr for male and 20gr for female per day.
* Patient has previous surgical bypass surgery for morbid obesity
* Patient has extensive small bowel resection
* Any major surgery in the past 3 months.
* Patient is a recipient of any organ transplant
* Pregnant or breastfeeding women.
* Patient allergic to acetaminophen
* Patients who are taking hepatotoxic drugs
* Patient, based on the opinion of the investigator, should not be enrolled into this study.
* Patients unable or unwilling to sign informed consent
* Patients that are participating in other clinical trials evaluating experimental treatments or procedures or have participated in a clinical trial in the past 3 months.
* Patient has not fasted for 8 hours.
* Patient has smoked on the day of the test.
* Patient that has taken drugs that can interfere with methacetin metabolism: fluvoxamine, amiodarone, ciprofloxacin, cimetidine, rifampin, carbamazepine within the last 24 hours.
* Patient has taken Tylenol or any other acetaminophen related medications within the past 24 hours.
* Patients that received any new medication in the last 48 hours.
* Patients that still suffer from any previous clinical intervention (e.g. biopsy)
* Have not consumed alcohol 24 hours prior the MBT and not consume on a regular basis more than 40gr for male and 20gr for female per day.
General
* Severe heart, pulmonary or renal disease.
* Patient has previous surgical bypass surgery for morbid obesity
* Patient has extensive small bowel resection
* Any major surgery in the past 3 months.
* Patient is a recipient of any organ transplant
* Pregnant or breastfeeding women.
* Patient allergic to acetaminophen
* Patients who are taking hepatotoxic drugs
* Patient, based on the opinion of the investigator, should not be enrolled into this study.
* Patients unable or unwilling to sign informed consent
* Patients that are participating in other clinical trials evaluating experimental treatments or procedures or have participated in a clinical trial in the past 3 months.
* Patient has not fasted for 8 hours.
* Patient has smoked on the day of the test.
* Patient that has taken drugs that can interfere with methacetin metabolism: fluvoxamine, amiodarone, ciprofloxacin, cimetidine, rifampin, carbamazepine within the last 24 hours.
* Patient has taken Tylenol or any other acetaminophen related medications within the past 24 hours.
* Patients that received any new medication in the last 48 hours.
* Patients that still suffer from any previous clinical intervention (e.g. -
* Have not consumed alcohol 24 hours prior the MBT and not consume on a regular basis more than 40gr for male and 20gr for female per day.
Minimum Eligible Age
18 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
Yes
Sponsors
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Meridian Bioscience, Inc.
INDUSTRY
Sponsor Role
collaborator
Hadassah Medical Organization
OTHER
Sponsor Role
lead
Locations
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Liver Unit Hadassah Medical Center
Jerusalem, , Israel
Site Status
Countries
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Israel
Other Identifiers
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METH-EX-610- HMO - CTIL
Identifier Type: -
Identifier Source: org_study_id