Urinary Proanthocyanidin-A2 as a Biomarker of Compliance to Intake of Cranberry Products
NCT ID: NCT01687114
Last Updated: 2014-12-15
Study Results
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View full resultsBasic Information
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COMPLETED
NA
5 participants
INTERVENTIONAL
2012-09-30
2014-04-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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cranberry juice
27% cranberry juice
cranberry juice
27% cranberry juice
Interventions
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cranberry juice
27% cranberry juice
Eligibility Criteria
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Inclusion Criteria
* aged 20-40 y
* body mass index (BMI): 18.5-25 kg/m2
* sexually active but not pregnant or planning to become pregnant
* no advance plans to discontinue use of hormonal contraceptives if they are taken
Exclusion Criteria
* History of a bilateral mastectomy
* Use of medications known or suspected to influence blood pressure
* cardiovascular diseases
* Gastrointestinal diseases,
* Renal or chronic kidney disease
* Endocrine disorders
* Rheumatologic diseases
* Immune deficiency conditions
* Active treatment for cancer of any type longer than 1 y
* Systolic blood pressure \>139 mmHg and/or diastolic blood pressure \>89 mmHg
* Regular use (more than 1x/wk) of any acid-lowering medications, laxatives (including fiber supplements) or anti-diarrheal medications
* Use of any antibiotics in the last month
* Regular use of systemic steroids, oral or injectable
* Gain or loss of more than 5% of body weight in the last 6 mo
* Any history of or known allergies to cranberries or cranberry products
* Regular use of any dietary supplements containing vitamins, minerals, herbal or other plant-based preparations, fish oil supplements or homeopathic remedies.
* Usual daily ethanol intake of equal and more than 2 drinks
* Cigarette smoking and/or nicotine replacement use.
* Strict vegetarians (vegans)
* Pregnancy
* Infrequent (\<3/wk) or excessive (\>3/d) number of regular bowel movements
* Inability to discontinue or refrain from ASA/NSAID or Tylenol use for 72 h prior to and for the duration of testing on Visits 2-13
* Participation in a clinical research trial within 60 d of their enrollment visit (Visit 2)
* Specific laboratory blood or urine analysis parameters of: Creatinine \>1.5 mg/dL, Electrolytes, calcium, phosphorous - out of normal ranges, ALT and AST \>1.5 nmol, Total bilirubin - above normal range, Fasting glucose ≥126 mg/dL, Total cholesterol \>239 mg/dL, Triglycerides ≥300 mg/dL, CBC: HCT \<32% for females, below normal range for males, WBC, PLT - out of normal range, hematuria, proteinuria
20 Years
40 Years
FEMALE
Yes
Sponsors
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Tufts University
OTHER
Responsible Party
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Oliver Chen
Research Scientist II
Principal Investigators
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Oliver Chen, PhD
Role: PRINCIPAL_INVESTIGATOR
Tufts University
Locations
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Jean Mayer USDA Human Nutrition Research Center on Aging
Boston, Massachusetts, United States
Countries
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Other Identifiers
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HNRC2785
Identifier Type: -
Identifier Source: org_study_id