Video Capsule Endoscopy Versus Colonoscopy in Patients With Melena and Negative Upper Endoscopy

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The Washington University

Status

Terminated

Conditions

Gastrointestinal Hemorrhage

Treatments

Procedure: Colonoscopy
Procedure: Video Capsule Endoscopy
Device: 1.0 X 2.5 cm 'pill' containing a camera

Study type

Interventional

Funder types

Other

Identifiers

NCT02609100
201507101

Details and patient eligibility

About

Acute gastrointestinal bleeding is a common medical problem. When patients with gastrointestinal bleeding present with melena (dark, tarry stool) the blood loss is usually originating in the upper gastrointestinal tract (esophagus, stomach or duodenum) and first step in evaluating the patient is an upper endoscopy; which allows direct visualization of the esophagus, stomach and duodenum. However, the cause of bleeding is located in the small bowel or colon in 20-30% of patients who present with melena. Traditionally colonoscopy has been the next test preformed if upper endoscopy does not identify the cause of melena/ gastrointestinal bleeding, however less than 25% of patients who present with melena have bleeding originating in the colon, and the remainder of patients have bleeding originating in the small intestine, which can only be fully evaluated with video capsule endoscopy (a pill camera which is swallowed and takes pictures while it travels thought the small bowel and colon). Currently patients only undergo video capsule endoscopy if colonoscopy does not identify the cause of bleeding. The investigators are preforming a randomized study which seeks to determine if colonoscopy or video capsule endoscopy is a better way to identify the cause of gastrointestinal bleeding in patients who present with melena and have normal findings on upper endoscopy. To do this the investigators will enroll patients who present with melena prior to their upper endoscopy and if the cause of bleeding is not identified at that time patients will be randomized to video capsule endoscopy (with the capsule being placed into the small bowel during the upper endoscopy) or next day colonoscopy.

Enrollment

4 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

• Inpatients >18 years of age presenting with lower gastrointestinal bleeding and have melenic stool

Exclusion criteria

  • Unable to provide written informed consent
  • A probable bleeding source is identified on upper endoscopy
  • Pregnancy or lactation
  • Swallowing Disorder
  • Unable to tolerate sedation or anesthesia due to medical co-morbidities
  • Uncorrected coagulopathy (platelet count <50,000, INR> 2, PTT> 2x upper limit of normal)
  • Known or suspected gastrointestinal obstruction or stricture
  • Cardiac pacemaker or other implanted electromedical device
  • Contraindication to bowel preparation

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

4 participants in 2 patient groups

Video Capsule Endoscopy
Active Comparator group
Description:
Randomization arm one is to video capsule endoscopy (VCE) a non-invasive procedure in which a patient swallows a disposable 1.0 X 2.5 cm 'pill' containing a camera electronically linked to equipment outside the patient which records images as it passes from the esophagus through the entire tract and is excreted in feces. It images the small intestine in areas beyond the reach of upper GI endoscopy and the terminal ileum and is similarly beyond the reach of colonoscopy. Its greatest use is in identifying points of bleeding and ulcers.
Treatment:
Device: 1.0 X 2.5 cm 'pill' containing a camera
Procedure: Video Capsule Endoscopy
Next Day Colonoscopy
Active Comparator group
Description:
Randomization arm two is to colonoscopy, a test that allows the doctor to look at the inner lining of the large intestine (rectum and colon). He or she uses a thin, flexible tube called a colonoscope to look at the colon.
Treatment:
Procedure: Colonoscopy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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