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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01998776
Other study ID # MISO-SB
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date April 2013
Est. completion date February 2018

Study information

Verified date January 2019
Source Chinese University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

ASA is the most commonly drug used worldwide for prevention of cardiovascular diseases. However, ASA is increasingly recognized as a culprit for small bowel bleeding. Small bowel bleeding is notoriously difficult to diagnose because it is beyond the reach of conventional endoscopy. The advent of wireless, video capsule endoscopy has revolutionized the visualization of small bowel. Capsule endoscopy is a pill that contains a tiny camera for capturing pictures of the small bowel after being swallowed. Currently, capsule endoscopy is a recommended noninvasive approach of identifying the source of small bowel bleeding.

Management of ASA-associated small bowel bleeding is a major clinical challenge since there is not a single effective treatment for small bowel ulcer, and continuation of ASA increases the risk of recurrent small bowel bleeding. However, discontinuation of ASA exposes patients to thrombotic complications. Suppression of prostaglandin synthesis is an important mechanism of ASA-induced small injury. Consistent with this theory, preliminary data from a case series showed that misoprostol, a prostaglandin analog, healed small bowel ulcers in ASA users. However, the efficacy of misoprostol in healing ASA-associated small bowel ulcers has not yet been confirmed by prospective randomized trials.

This double-blind clinical trial tests the hypothesis that misoprostol can heal small bowel ulcers in Aspirin users complicated by small bowel bleeding.


Description:

ASA is the most commonly drug used worldwide for prevention of cardiovascular diseases. However, ASA is increasingly recognized as a culprit for small bowel bleeding. The latter condition manifests as overt bleeding (i.e., passing black or bright red stool) or occult blood loss (i.e., normal stool but progressive decrease in hemoglobin level), with normal findings in the stomach and colon. Small bowel bleeding is notoriously difficult to diagnose because it is beyond the reach of conventional endoscopy. The advent of wireless, video capsule endoscopy has revolutionized the visualization of small bowel. Capsule endoscopy is a pill that contains a tiny camera for capturing pictures of the small bowel after being swallowed. Currently, capsule endoscopy is a recommended noninvasive approach of identifying the source of small bowel bleeding.

The problem of small bowel bleeding is increasingly recognized, partly because the use of ASA is rising. In a regional hospital in Hong Kong, we diagnose about 100 cases of ASA-associated small bowel overt bleeding/occult blood loss each year. In a prospective cohort study we found that among ASA users with a history of small bowel bleeding, the risk of recurrent small bowel bleeding is 4 times higher in patients who continued to use ASA than in those who discontinued ASA.

Management of ASA-associated small bowel bleeding is a major clinical challenge for two reasons. First, there is not a single effective treatment for small bowel ulcer. Unlike peptic ulcers, injury to the small bowel is acid-independent. Thus, conventional stomach protective drugs cannot heal or prevent small bowel ulcers in ASA users. Neither can switching to other non-ASA anti-platelet drugs reduce the risk of bleeding. Second, we have shown that continuation of ASA increases the risk of recurrent small bowel bleeding. However, discontinuation of ASA exposes patients to thrombotic complications. Currently, there is no local or international guideline on the management of ASA-associated small bowel bleeding.

Suppression of prostaglandin synthesis is an important mechanism of ASA-induced small injury. Consistent with this theory, preliminary data from a case series showed that misoprostol, a prostaglandin analog, healed small bowel ulcers in ASA users. However, the efficacy of misoprostol in healing ASA-associated small bowel ulcers has not yet been confirmed by prospective randomized trials.


Recruitment information / eligibility

Status Completed
Enrollment 82
Est. completion date February 2018
Est. primary completion date January 22, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria:

1. Suspected small bowel overt bleeding - melena or hematochezia with normal upper endoscopy and colonoscopy

2. Suspected small bowel occult blood loss - defined as a significant decrease in hemoglobin (= 2g/dL), with normal upper endoscopy and colonoscopy, confirmed iron deficiency anemia, and absence of other identifiable causes for hemoglobin decrease (e.g. fluid overload, progressive renal failure, malnutrition, or other hematological disorders such as hemolysis or malignancies)

3. Continuous use of ASA for the duration of the trial

4. Age = 18

5. Written informed consent obtained

Exclusion criteria:

Patients are excluded if they have one or more of the following conditions

1. Increased risk of capsule retention (e.g. Gastric outlet obstruction, bypass surgery, Crohn's disease or suspected small bowel stricture)

2. Abnormal findings on upper endoscopy (e.g. Esophageal varices, grade C or D erosive esophagitis, vascular malformations, ulcer, =5 erosions, neoplasms) or colonoscopy (e.g. cancer, polyps > 1cm, inflammatory bowel disease, vascular malformations, bleeding hemorrhoids or diverticular disease)

3. Unable to swallow the video capsule

4. Terminal illness

5. Concomitant use of NSAIDs, sucralfate, rebamepide, anticoagulants, corticosteroids (prednisolone > 7.5mg daily or equivalent), and iron supplement

6. Pregnancy or women of child-bearing age without regular use of contraception

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Misoprostol
Misoprostol 200ug four times daily
Placebo
Placebo Starch four times daily

Locations

Country Name City State
China Prince of Wales Hospital Hong Kong
Japan Department of Gastroenterology, Osaka City University Graduate School of Medicine Osaka

Sponsors (1)

Lead Sponsor Collaborator
Chinese University of Hong Kong

Countries where clinical trial is conducted

China,  Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complete healing of small bowel ulcers The primary outcome is complete healing of small bowel ulcers in 8 weeks 8 weeks
Secondary Change in numbers of ulcer/erosions, and hemoglobin level Secondary outcomes include change in the numbers of ulcer/erosions and change in blood hemoglobin level from baseline 8 weeks
See also
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Completed NCT01278550 - Prevention of Recurrent Ulcer Bleeding in High-risk Users of Low-dose Aspirin N/A
Completed NCT04239118 - New Technologies for Endoscopic Treatment of Bleeding Gastroduodenal Ulcers N/A
Completed NCT05227833 - Vonoprazan Efficacy to Prevent Post Variceal Band Ligation Ulcer Phase 3