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Study of Metoclopramide in Small Bowel Capsule Endoscopy

A

Ascension Health

Status and phase

Completed
Phase 4

Conditions

Pill Capsule Endoscopy Completion Rates

Treatments

Drug: Placebo
Drug: Metoclopramide

Study type

Interventional

Funder types

Industry

Identifiers

NCT01630109
GRMC120006

Details and patient eligibility

About

Patients undergoing small bowel capsule endoscopy will be randomized into 3 study groups to either receive 5 mg of metoclopramide, 10 mg of metoclopramide, or a placebo 30 minutes prior to swallowing the Pill Cam. This is a randomized, double-blind, placebo-controlled design. The outcomes to be assessed are capsule study completion rates, gastric transit time, small bowel transit time, and the effect of diabetes on pill capsule completion rates. The purpose of the study is to assess if metoclopramide given prior to pill capsule endoscopy has any effect on pill capsule completion rate, gastric transit time, small bowel transit time, and pill capsule completion rates in diabetes.

Full description

Pill Capsule Endoscopy allows Gastroenterologists to visualize the mucosa of the small bowel beyond the reach of any endoscope and to an extent never before possible. It involves the ingestion of a small pill camera approximately the size of a large vitamin. 8 hours of images are transmitted to a sensor worn around the patient's waist. At the conclusion of the test, these images are downloaded to a computer for physician review. Meanwhile, the PillCam™ passes naturally through the digestive system and does not require retrieval.

Many of these pill capsule studies are incomplete due to failure of the pill capsule to reach the colon. Metoclopramide (brand name Reglan) is an anti-emetic that also has known pro-motility effects in the GI tract. The thought behind this study is that metoclopramide will increase the rate of passage of the pill capsule through the GI tract allowing a higher completion rate of the pill capsule studies.

Patients scheduled for pill capsule endoscopy will be approached on the morning of their procedure to inform them of the research study. After proper consent is obtained the patient will receive either 5 mg Metoclopramide, 10 mg Metoclopramide, or a placebo pill 30 minutes prior to their pill capsule study. The pill capsule camera records 8 hours worth of data. The patient will return at the conclusion of their study to turn in their recorder. The ordering gastroenterologist will then read the study. Information regarding pill capsule completion (pill capsule goes through the ileocecal valve), gastric transit time, and small bowel transit time will then be recorded and analyzed.

Enrollment

5 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Men and women over the age of 18 undergoing pill capsule endoscopy to investigate unexplained rectal bleeding, anemia, iron deficiency, abdominal pain, altered bowel habits, and/or weight loss.

Exclusion criteria

  • Inability to sign consent for research participation
  • Inability to swallow PillCam™, placebo, or metoclopramide capsule
  • Known hypersensitivity/allergy to metoclopramide
  • Active congestive heart failure or respiratory failure requiring ventilator assistance
  • Presence of cardiac pacemaker or implanted electromedical device
  • Known bowel obstruction/stricture/fistula or intrauterine pregnancy
  • Known history of Whipple procedure (pancreaticoduodenectomy), Billroth II surgery (partial gastrectomy with gastrojejunostomy), or gastric bypass surgery due to risk of capsule retention in a blind intestinal limb necessitating surgical retrieval
  • Known history of seizure disorder, renal failure requiring dialysis, or pheochromocytoma
  • Lactating women

Trial design

5 participants in 3 patient groups, including a placebo group

Metoclopramide 5 mg
Active Comparator group
Description:
Pro-motility agent
Treatment:
Drug: Metoclopramide
Metoclopramide 10 mg
Active Comparator group
Description:
Pro-motility agent
Treatment:
Drug: Metoclopramide
Placebo control
Placebo Comparator group
Description:
Placebo to be used as the control group
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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