Effects of Oral PEG 3350 on Electrolyte Balance

NCT ID: NCT00868985

Last Updated: 2009-03-25

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 114 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-01-31

Brief Summary

The study is to evaluate the influence of three different doses of PEG 3350 with or without electrolytes on the electrolyte balance in patient volunteers with confirmed chronic constipation.

Conditions

Chronic Constipation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

PEG 3350 plus electrolytes

Patients were dosed with PEG 3350 with electrolytes

Group Type: EXPERIMENTAL

PEG 3350 plus electrolytes

Intervention Type: DRUG

Each patient was treated with PEG 3350 with electrolytes for 10 days at a dose of either one, two or three sachets per day.

PEG 3350 without electrolytes

Patients were dosed with PEG 3350 without electrolytes

Group Type: EXPERIMENTAL

PEG 3350 without electrolytes

Intervention Type: DRUG

Each patient was treated with PEG 3350 for 10 days at a dose of either one, two or three sachets per day.

Interventions

PEG 3350 plus electrolytes

Each patient was treated with PEG 3350 with electrolytes for 10 days at a dose of either one, two or three sachets per day.

Intervention Type: DRUG

PEG 3350 without electrolytes

Each patient was treated with PEG 3350 for 10 days at a dose of either one, two or three sachets per day.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. The subjects written informed consent must be obtained prior to inclusion.

2. Male and female patients between 18 and 70 years of age with confirmed chronic constipation after the run-in period; this is defined as patients who have recorded in their diaries less than 3 bowel motions/week plus one of the following symptoms:

Straining during at least 25% of defecations Lumpy or hard stools with at least 25% of defecations Sense of incomplete evacuation with at least 25% of defecation Sensation of ano-rectal blockage with at least 25% of defecation Manula manoeuvres of facilitate at least 25% of defecation

3. Willing and able to follow the entire procedure and to comply with the study instructions.

4. For the subgroup of patient volunteers taking ACE-inhibitors (36 subjects): A history of hypertension, with blood pressure controlled to acceptable levels by a stable regimen of ACE-inhibitors.

Exclusion Criteria

1. Participation in a clinical research study involving investigational drugs or dosage forms within the previous 3 months.

2. Subjects who have previously been enrolled in this study.

3. Subjects who are currently or have a history of abuse of alcohol, non-medical drugs, medicinal drugs or other substance abuse eg solvents.

4. Major surgery in within the last 12 months.

5. Malignant tumors within the last 5 years.

6. Uncontrolled blood pressure or terminal cardiac, liver and/or kidney diseases.

7. Clinical relevant acute gastrointestinal tract disease, including evidence of intestinal perforation or obstruction, paralytic ileus, toxic megacolon, severe inflammatory conditions.

8. Acute urinary tract conditions, including cystitis.

9. Patients with diagnosis or evidence of the following diseases: Hypothyroidism, diabetes mellitus, porphyria, pituitary gland insufficiency, pheochromocytoma, glucagonoma, neurological diseases (eg Hirschprung disease, neurofibromatosis, Chagas disease, stroke, autonomous neuropathy, intestinal pseudoobstruction, Multiple sclerosis, medullar injury, Parkinson disease, Shy-Drager syndrome), collagenosis, vasculitis, myopathy (e.g. sclerodermatitis, amyloidosis, dermatomyositis), intoxication with heavy metals (e.g. Pb, As, Hg)

10. Concomitant medication:

1. Use of any oral purgatives/laxatives and prokinetics within the last 14 days prior to dosing.

2. Use of any opioids, anti-cholinergics, tricyclic anti-depressants, MAOIs, Fe preparations, within the 4 weeks prior to dosing.

3. Use of any Ca-antagonists, Beta-blockers or diuretics within the last 4 weeks prior to dosing.

4. other medication which in the opinion of the Investigator could interfere with the principal function of the GI tract.

11. Subject unable to provide written consent.

12. Failure to satisfy the Investigator of fitness to participate for any other reason, including suspected non-compliance.

13. Women of childbearing potential, who are not using and not willing to use medically reliable methods of contraception for the entire study duration, unless they are surgically sterilised/hysterectomised or any other criteria considered sufficiently reliable by the Investigator in individual cases.

14. Patients with electrolytes disturbances or clinical signs of dehydration.

15. Positive test at screening for HIV or hepatitis.

16. Any clinically significant abnormal test results.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Norgine

INDUSTRY

Sponsor Role: lead

Responsible Party

Norgine Ltd

Principal Investigators

Hans-Jürgen Gruss, MD

Role: STUDY_DIRECTOR

Norgine

Rodica Cinca, MD

Role: PRINCIPAL_INVESTIGATOR

IFE Human Pharmacology

Locations

IFE Human Pharmacology

Timișoara, , Romania

Countries

Romania

Other Identifiers

PEG-01/2007(ELE)

Identifier Type: -

Identifier Source: org_study_id