Efficacy and Safety Study of the Effect of Dose-Titration of Prucalopride for The Treatment of Chronic Constipation

NCT00577018 | Completed Phase 3

• 1 other identifier: PRU-USA-25
• Study Type: interventional
• Target: 755
• Locations: 0 countries
• Sites: N/A

Brief Summary

The purpose of this study is to determine the safety profile of 4 mg prucalopride in the treatment of chronic constipation.

Conditions

Constipation

Outcome Measures

Primary Outcomes (1)

• Proportion of patients with an average of ≥3 SCBM/week

  4 weeks

Secondary Outcomes (1)

• Proportion of patients with an average increase of ≥1 SCBM/week

  4 weeks

Study Arms (3)

1

ACTIVE COMPARATOR

Drug: Prucalopride

2

ACTIVE COMPARATOR

Drug: Prucalopride

3

PLACEBO COMPARATOR

Other: Placebo

Interventions

Prucalopride DRUG

4 mg o.d.

Also known as: Resolor

1

Placebo OTHER

o.d.

3

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male and non-pregnant, non-breast feeding female subjects at least 18 years of age (no upper age limit);
• History of constipation. The subject reported having on average, 2 or fewer spontaneous bowel movements per week that resulted in a feeling or sensation of complete evacuation, as well as the occurrence of one or more of the following for at least 6 months before the selection visit: very hard (little balls) and/or hard stools for at least a quarter of the stools; sensation of incomplete evacuation following at least a quarter of the stools; or straining at defecation at least a quarter of the time. The above criteria only applied to spontaneous bowel movements, (i.e., not preceded within a period of 24 hours by the intake of a laxative or use of an enema). A subject who never had spontaneous bowel movements was considered to be constipated and therefore eligible for the trial;
• Constipation that was functional (i.e., not secondary to other causes);
• Willingness and ability to fill out own diary and questionnaires;
• Written informed consent, signed by the subject or legally acceptable representative and by the investigator; and
• Availability for follow-up during the trial period, as determined in the protocol.

You may not qualify if:

• Subjects in whom constipation was thought to be drug-induced or who were using any disallowed medication;
• Subjects suffering from secondary causes of chronic constipation. For example:
• Endocrine disorders: insulin-dependent diabetes mellitus; hypopituitarism; hypothyroidism; hypercalcemia; pseudo-hypoparathyroidism; pheochromocytoma; or glucagon-producing tumors. Endocrine disorders controlled by appropriate medical therapy were not excluded, with the exception of insulin-dependent diabetes mellitus Metabolic disorders: porphyria; uremia; hypokalemia; or amyloid neuropathy. Metabolic disorders controlled by appropriate medical therapy were not excluded
• Presence of megacolon/megarectum or a diagnosis of pseudo-obstruction;
• Constipation as a result of surgery;
• Known or suspected organic disorders of the large bowel (i.e., obstruction, carcinoma, or inflammatory bowel disease). Results of a barium enema with flexible sigmoidoscopy or of a colonoscopic examination performed within the last 12 months were needed to rule out organic disorders. An examination performed within the last 3 years was acceptable, if the examination had been performed for an evaluation of constipation, if there was no history or evidence of weight loss, anemia, or rectal bleeding, and if the subject had had three consecutively negative stool occult blood tests at screening. Subjects with polyps discovered by colonoscopy that were untreated (i.e., by polypectomy) were to be excluded;
• Presence of severe and clinically uncontrolled cardiovascular, liver or lung disease, neurologic or psychiatric disorders (including active alcohol or drug abuse);
• Clinically significant cancer within the past 5 years;
• Known HIV-positive status or AIDS;
• Impaired renal function;
• Clinically significant abnormalities of hematology, urinalysis or blood chemistry;
• Females of child-bearing potential without adequate contraceptive protection during the trial. Oral contraceptives, Depo-Provera®, or Norplant®) must have been used for at least 3 months prior to randomization. I.U.D.'s, sterilization, or a double-barrier method were other acceptable methods of birth control;
• Treatment with an investigational drug in the 30 days preceding the run-in phase of the trial; and
• Previous treatment with either R093877 (prucalopride hydrochloride) or R108512 (prucalopride succinate).

Sponsors & Collaborators

• Movetis: lead

MeSH Terms

Conditions

Constipation

Interventions

prucalopride

Condition Hierarchy (Ancestors)

Signs and Symptoms, Digestive; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Officials

• John F Johanson, MD, MSc

  Private Practice

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: December 17, 2007
• First Posted: December 19, 2007
• Study Start: August 1, 1998
• Primary Completion: September 1, 1999
• Study Completion: September 1, 1999
• Last Updated: May 29, 2008

Record last verified: 2007-12