Prucalopride Prior to Small Bowel Capsule Endoscopy
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|ClinicalTrials.gov Identifier: NCT02806206|
Recruitment Status : Unknown
Verified July 2016 by University of British Columbia.
Recruitment status was: Not yet recruiting
First Posted : June 20, 2016
Last Update Posted : July 15, 2016
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Small bowel capsule endoscopy is a test used to investigate for any abnormalities in the small bowel. The small bowel is about 4 meters long. The battery time of the capsule is about 8 hours. During this time the capsule takes pictures as it passes through the small bowel. In about 15-20% of capsule tests the battery expires before the capsule passes through the entire small bowel into the colon. Incomplete tests indicate that a variable portion of small bowel was not visualized. Incomplete tests are associated with potential missing of abnormalities in the portion of small bowel that was not reached. The capsule test may often required to be repeated but the problem of incomplete examination may persist. At present no medication has been approved to increase the rate of complete capsule tests.
Prucalopride is a medication that has been approved in Canada and Europe for the treatment of chronic idiopathic constipation. Animal and human studies suggested that prucalopride may enhance the movement of the stomach and the small bowel. A recent presentation at a medical meeting suggested that prucalopride may accelerate the passage of the capsule camera through the small bowel without increasing the chance to miss a lesion in the small bowel.
The purpose of this study is to asses if the administration of a single dose of prucalopride is going to decrease the time required by the capsule to move through the small bowel.
|Condition or disease||Intervention/treatment||Phase|
|Gastrointestinal Hemorrhage Crohn Disease Celiac Disease Intestinal Diseases Inflammatory Bowel Diseases||Drug: Prucalopride Drug: Placebo||Phase 4|
Capsule Endoscopy is now the first test to investigate for small bowel disease. Clinical conditions in which capsule endoscopy can be useful include gastrointestinal bleeding of unclear source, Crohn's disease, celiac disease and suspected small bowel tumors. Optimal diagnostic yield of the capsule endoscopy depends not only on adequate small bowel visualization, but also on the completion of small bowel examination. In approximately 15-20% of capsule studies, the capsule fails to pass through the small bowel into the colon because of the limited battery time which is about 8 hours. This means that a lesion or an abnormality can be missed in the portion of the small bowel that was not reached by the capsule. As a result, the capsule endoscopy test may often need to be repeated.
Multiple factors have been associated with the prolongation of the time required for the capsule to pass through the small bowel including hospitalization, prior small bowel surgery, diabetes and advanced age in addition to the prolongation of the time required for the capsule to pass through the stomach. Interventions to shorten small bowel transit time are required to increase capsule small bowel completion rates. At present there is no drug approved to shorten the small bowel transit time.
Prucalopride is a drug that has been approved for use in patients with chronic constipation. Prucalopride works on special receptors in the gut and stimulate the gut movement. There are basic and clinical studies suggesting that prucalopride may accelerate the movement of the stomach and the small bowel. Therefore, prucalopride may accelerate the passage of the capsule through the small bowel and increase the capsule completion rates. The investigators of this trial recently presented their experience of prucalopride use prior to capsule endoscopy at a medical meeting. Compared to a retrospective control group who did not receive prucalopride, prucalopride accelerated the passage of the capsule through the small bowel. There was no decrease in the diagnostic yield in the group who received prucalopride.
In this clinical trial, the investigators aim to investigate the effect of prucalopride on the small bowel transit time, by performing a randomized placebo controlled trial. Patients undergoing small bowel capsule endoscopy tests will be randomized to a single dose of prucalopride ingested at the time of capsule endoscopy ingestion, or a placebo pill. The primary objective of this study is to examine if the administration of a single dose of prucalopride shortens small bowel transit time compared to placebo. The secondary objectives include examining the effect of prucalopride on gastric transit time, small bowel capsule endoscopy completion rate and the capsule diagnostic yield. The placebo group is used in this clinical trial because there is no drug proven to be effective to shorten the small bowel transit time.
Based on the experience of the investigators, the average small bowel transit time for patients who were given prucalopride was 143 minutes. In the retrospective control group, the small bowel transit time was 229 minutes with a standard deviation of 90 minutes. Based on a presumed 20% minimal clinically important difference in small bowel transit time, the investigators determined a total of 122 participants will be required, equally divided between the two study arms.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||122 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Investigator, Outcomes Assessor)|
|Official Title:||The Effect of Prucalopride on Small Bowel Transit Time in Patients Undergoing Capsule Endoscopy: A Randomized Controlled Trial|
|Study Start Date :||July 2016|
|Estimated Primary Completion Date :||May 2017|
|Estimated Study Completion Date :||May 2017|
Experimental: Drug: Prucalopride
A single 2 mg dose of prucalopride before ingesting the capsule endoscopy pill.
A single 2 mg oral dose of prucalopride will be given to each study participant just before the ingestion of the capsule endoscopy pill.
Other Name: Restoran
Placebo Comparator: Drug: Placebo
A placebo pill just before ingesting the capsule endoscopy pill.
A single dose of a placebo pill will be given to each study participant just before the ingestion of the capsule endoscopy pill.
Other Name: Sugar pill
- Small bowel transit time [ Time Frame: 10 hours post dose ]The calculated time from the first duodenal image to the first cecal image. The capsule images will be collected when the capsule is finished recording, approximately 10 hours post-dose.
- Gastric transit time [ Time Frame: 10 hours post dose ]The calculated time from the first gastric image to the first duodenal image. The capsule images will be collected when the capsule is finished recording, approximately 10 hours post-dose.
- Small bowel completion rate [ Time Frame: 10 hours post dose ]The proportion of capsule studies in which the capsule reached the cecum. The capsule images will be collected when the capsule is finished recording, approximately 10 hours post-dose.
- Diagnostic yield [ Time Frame: 10 hours post dose ]The findings were considered diagnostic if the observed finding could explain the signs/symptoms of the patient and helped plan further management or were later confirmed by other modalities. The capsule images will be collected when the capsule is finished recording, approximately 10 hours post-dose.
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|Ages Eligible for Study:||19 Years and older (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Appropriate indication for small bowel capsule endoscopy.
- Age 19 or older.
- Previous partial or complete gastric resection.
- Previous small bowel surgery in which a small bowel resection has been performed or the normal anatomy has been altered.
- Presence of ileostomy.
- The requirement for endoscopic placement of the capsule endoscopy pill because of dysphagia or gastroparesis.
- Severe renal impairment, defined by the requirement for dialysis.
- Pregnancy or breast feeding.
- Clinical or radiological suspicion of small bowel obstruction.
- Simultaneous use of a prokinetic agent within 5 days of the capsule endoscopy examination.
- Clinical hypo- or hyperthyroidism.
- Known hypersensitivity to the study drug.
- Unwillingness to sign informed consent.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02806206
|Contact: Fergal Donnellan, MD||6048755474||Fergal.Donnellan@vch.ca|
|Contact: Nazira Chatur, MDemail@example.com|
|Canada, British Columbia|
|Vancouver General Hospital|
|Vancouver, British Columbia, Canada, V5Z 1M9|
|Principal Investigator:||Fergal Donnellan, MD||Division of Gastroenterology, University of British Columbia|
|Study Director:||Majid Alsahafi, MD||Division of Gastroenterology, University of British Columbia|
|Responsible Party:||University of British Columbia|
|Other Study ID Numbers:||
|First Posted:||June 20, 2016 Key Record Dates|
|Last Update Posted:||July 15, 2016|
|Last Verified:||July 2016|
|Individual Participant Data (IPD) Sharing Statement:|
|Plan to Share IPD:||No|
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