Efficacy and Safety Study of Prucalopride for the Treatment of Chronic Constipation
NCT ID: NCT00617513
Last Updated: 2008-05-29
Study Results
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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COMPLETED
PHASE2
174 participants
INTERVENTIONAL
1995-03-31
1996-03-31
Brief Summary
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Hypothesis:
Prucalopride 1 and 2 mg are safe and effective for the treatment of chronic idiopathic constipation whereas 0,5 mg is a suboptimal dose.
Detailed Description
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Phase 1 is a run-in period of 4 weeks duration, during which the bowel habit is documented and the existence of constipation confirmed. At the start of this period all existing laxative medication is withdrawn but patients will be instructed not to change their dietary habits, in particular their fibre intake during the trial. Patients will enter the double-blind phase if constipation has been shown to be present during the run-in period.
If the definition of constipation was not met during the 4 weeks of the run-in period, double-blind treatment will not be started.
Phase 2 is a double-blind, randomized, placebo-controlled phase, in which patients will be treated for 4 weeks with either 0.5 mg, 1 mg or 2 mg of R093877 or placebo given once daily (one capsule is taken before breakfast).
Patients admitted to the double blind treatment period will be randomly allocated to one of the 4 treatment arms.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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1
Prucalopride
0.5 mg once daily
2
Prucalopride
1 mg o.d.
3
Prucalopride
2 mg o.d.
4
Placebo
o.d.
Interventions
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Prucalopride
0.5 mg once daily
Placebo
o.d.
Prucalopride
1 mg o.d.
Prucalopride
2 mg o.d.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* History of constipation i.e., the patient reported the occurrence of TWO OR MORE of the following criteria for at least 6 months before the selection visit :
1. two or fewer spontaneous\* bowel movements in a week.
2. lumpy (scyballae) and/or hard stools at least a quarter of the stools.
3. sensation of incomplete evacuation following at least a quarter of the stools.
4. straining at defaecation at least a quarter of the time. \*A bowel movement was considered spontaneous if it was not preceded by the intake of a laxative agent within a period of 12 hours. An amendment was made changing this period to 24 hours. Moreover, the amendment stated: "Patients who never opened their bowels spontaneously would be considered constipated and eligible to enter the double-blind phase of the trial, whether or not the above mentioned criteria were met for laxativa/enemas induced stools".
* Constipation causing disability; the patient's occupational, social and recreational activities were governed by his/her constipation and efforts to attain relief.
* Normal electromyographic inhibition pattern of the external anal sphincter during straining (clinical and/or electromyographic and/or manometric evidence is acceptable).
* Absence of organic abnormalities of the colon on barium enema or on total colonoscopic examination. This criterion was amended to: "If complaints of constipation were of recent onset,i.e., had been present for 6 months to 1 year, results of a colonoscopic examination performed within the last 12 months were needed. If complaints of constipation had been present for more than one year, results of an endoscopic examination performed within the past three years were acceptable".
* Poor results with laxative treatment and diet counselling.
* Constipation of a functional, i.e., idiopathic nature.
* Availability of the patient's written informed consent.
* Patient available for follow-up during the trial period as determined in the protocol.
Exclusion Criteria
* Presence of secondary causes of constipation, for instance: endocrine disorders, metabolic disorders, neurologic disorders.
* Congenital megacolon/megarectum.
* History of previous abdominal surgery other than hysterectomy, surgery for Meckel's diverticle,appendicectomy, cholecystectomy, inguinal repair, splenectomy, nephrectomy or fundoplication.
* Known or suspected organic disorders of the large bowel, i.e., obstruction, carcinoma or inflammatory bowel disease.
* Active proctological conditions which were thought to be responsible for constipation.
* Evidence of a non-relaxing pelvic floor ("anismus") as the main cause of constipation.
* Clinically significant ECG abnormalities.
* Known illnesses or conditions which might interfere in any way with the adequate assessment of the drug under study, such as severe cardiovascular or lung disease, neurologic or psychiatric disorders, alcoholism, cancer or AIDS.
* Impaired renal function
* Presence of a serum amylase-, a serum glutamic-oxaloacetic transaminase (SGOT) or a serum glutamic-pyruvic transaminase (SGPT) concentration of \> 2 times the upper limit of normal.
* Clinically significant abnormalities of blood chemistry, haematology or urinalysis at selection.
* Pregnancy or wish to become pregnant during the course of the study. - Breast feeding.
* Investigational drug received in the 30 days preceding the trial.
* Known use of street drugs e.g., marijuana, cocaine etc.
* Unability or unwillingness to return for required follow-up visits.
* Reliability and physical state preventing proper evaluation of a drug trial.
18 Years
70 Years
ALL
No
Sponsors
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Movetis
INDUSTRY
Responsible Party
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Movetis
Principal Investigators
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Marc Van Outryve, MD
Role: PRINCIPAL_INVESTIGATOR
Jan Palfijn Hospital
References
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Emmanuel A, Cools M, Vandeplassche L, Kerstens R. Prucalopride improves bowel function and colonic transit time in patients with chronic constipation: an integrated analysis. Am J Gastroenterol. 2014 Jun;109(6):887-94. doi: 10.1038/ajg.2014.74. Epub 2014 Apr 15.
Other Identifiers
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PRU-INT-1
Identifier Type: -
Identifier Source: org_study_id