Overview

Assessment of Gastric Emptying Speed in Patients Who Experience Diarrhea Following a Trigger Meal

Status:
Withdrawn
Trial end date:
2011-01-01
Target enrollment:
0
Participant gender:
All
Summary
The rapid diarrhea that patients experience who have diarrhea occurring after eating specific foods may be causing a "physiologic gastric dumping syndrome". This means that rather than the food being kept in the stomach for normal digestion, it rapidly goes into the small intestine and diarrhea occurs. This study is designed to measure how fast the food empties from the stomach when a person with this problem consumes a "regular diet", compared to a meal with a "triggering substance". Each participant will swallow a radio frequency capsule that with the different meals that will show how fast the food is traveling through the intestines in the different situations.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Money, Mary E., M.D.
Criteria
Inclusion Criteria:

1. The patient must have been diagnosed as having post prandial diarrhea for at least 5
years by his/her primary care physician or gastroenterologist and is believed to have
no other medical condition that would cause this medical problem. Each person must be
over 18 years old and have negative testing for Celiac Disease, a normal colonoscopy
within 5 years of enrollment, and a normal Hgb and sedimentation rate within 6 months
of enrollment in the trial.

2. The patient has provided documented written informed consent/authorization prior to
initiation of any study-related procedure.

3. In addition, each patient must report experiencing the onset of urgent defecation
within 1 hours of eating a specific trigger which is reproducible at least 90% of the
time when consume.

4. The patient must be willing to comply with all of the study protocol.

Exclusion Criteria:

1. The patient has had any rectal bleeding or bloody stools within the last 2 years not
completely evaluated by a physician. If rectal bleeding has occurred, and the patient
wants to be considered for the study, the diagnostic workup must have clearly
identified the etiology for the bleeding and excluded the medical conditions listed
under 3 below. The patient must be willing to allow the Study team to obtain these
records for verification of the diagnosis.

2. The patient has nocturnal bowel movements.

3. The patient has been diagnosed with or has a family history of any of the following:
ulcerative colitis, Crohn's Disease, celiac disease, sprue, other inflammatory bowel
disease or has a positive test for celiac disease on screening lab and has not had a
full investigation performed to exclude celiac disease.

4. The patient has had unexplained anorexia or weight loss of more than 10% of body
weight within 12 months of onset of study.

5. Prior GI surgery except of uncomplicated appendectomy and laparoscopic cholecystectomy
or history of bowel obstruction or symptoms suggestive of such within the past 2
years.

6. The patient reports daily use of laxatives or stool softeners; use of fiber
supplementation is permitted.

7. The patient is currently using pancrealipase. Previous use of pancrealipase in the
past is allowed, but patients must be off either of the medication for at least 1 week
or until the patient's symptoms of post prandial diarrhea returns before participating
in the study.

8. Use of implanted or ambulatory electromechanical medical devices such as pacemakers,
insulin pumps, and infusion pumps.

9. History of gastroparesis or chronic use of reglan.

10. Dysphagia to solid food and pills.

11. Previous gastro-esophageal surgery including vagotomy, fundoplication, gastric bypass
or ulcer surgery.

12. Tobacco use within eight hours prior to capsule ingestion and during the 8 hour
monitoring time.

13. Alcohol use within 24 hours prior to capsule ingestion and throughout the entire
monitoring period (up to 72 hours).

14. BMI > 35

15. Female of childbearing age who is not practicing birth control and/or is pregnant or
lactating. (Confirm with urine pregnancy test).