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Rifaximin and Misoprostol Combination Therapy for Healing of Small Bowel Ulcers in Aspirin Users

Primary Purpose

Small Bowel Disease, Rifaximin

Status
Unknown status
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
Rifaximin
Placebo oral tablet
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Small Bowel Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Suspected small bowel overt bleeding - melena or hematochezia with or without a source of bleeding from gastroscopy and colonoscopy or suspected small bowel occult blood loss - defined as a significant decrease in hemoglobin (> 2g/dL), without a source of bleeding from gastroscopy 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)
  • Continuous use of aspirin for the duration of the trial
  • Age ≥ 18
  • Written informed consent obtained

Exclusion Criteria:

  • Increased risk of capsule retention (e.g. gastric outlet obstruction, bypass surgery, Crohn's disease or suspected small bowel stricture)
  • Abnormal findings on gastroscopy that may account for bleeding episode: clean-based ulcer >2 cm or >5 erosions, esophageal varices, grade C or D erosive esophagitis, vascular malformations
  • Unable to swallow the capsule endoscopy
  • Terminal illness
  • Concomitant use of NSAIDs, sucralfate, rebamepide, antibiotics, corticosteroids (prednisolone >7.5 mg daily or equivalent), and iron supplement
  • Pregnancy (except LMP within 7 days) or women of child-bearing age without regular use of contraception
  • Contraindications to colonoscopy or capsule endoscopy

Sites / Locations

  • Beijing Friendship Hospital, Capital Medical UniversityRecruiting
  • Prince of Wales HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Rifaximin

Rifaximin Placebo

Arm Description

ASA daily + misoprostol + Rifaximin (Rifaximin group)

ASA daily + misoprostol + Placebo Rifaximin (Placebo group)

Outcomes

Primary Outcome Measures

Healing of small bowel ulcers
Capsule endoscopy will be performed to check if there is complete healing of small bowel ulcers, with or without red spots.

Secondary Outcome Measures

Change in numbers of ulcer/erosions
Change in numbers of ulcer/erosions from baseline within and between groups
Change in blood hemoglobin level
Change in blood hemoglobin level from baseline within and between groups

Full Information

First Posted
May 19, 2019
Last Updated
June 29, 2020
Sponsor
Chinese University of Hong Kong
Collaborators
Beijing Friendship Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03962283
Brief Title
Rifaximin and Misoprostol Combination Therapy for Healing of Small Bowel Ulcers in Aspirin Users
Official Title
Rifaximin and Misoprostol Combination Therapy for Healing of Small Bowel Ulcers in Aspirin Users With Small Bowel Bleeding: A Double Blind Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 2, 2019 (Actual)
Primary Completion Date
June 30, 2022 (Anticipated)
Study Completion Date
June 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
Collaborators
Beijing Friendship Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Investigators have previously shown that misoprostol can heal small bowel ulcers in aspirin users with small bowel bleeding. However, the rate of small-bowel mucosal healing was low with use of misoprostol alone. There is evidence to suggest that bacteria contribute to the development aspirin-induced ulcers and antibiotics may be useful in its treatment. Rifaximin, a non-absorbed oral antibiotic that target the gastrointestinal tract have been shown to be safe and effective in a few other gastrointestinal conditions. Small bowel capsule is the most sensitive and non-invasive way to investigate the small bowel. It plays an important role in obscure GIB investigations. Aims: The aim of this randomized study is to test the hypothesis that misoprostol combined with rifaximin is superior to misoprostol alone for healing of small bowel ulcers in aspirin users complicated by small bowel bleeding. Study design: 8-week double-blind randomized trial
Detailed Description
Aspirin is one of the most commonly prescribed drugs worldwide It is widely used as the first line agent for prevention and treatment of heart diseases and stroke. It is well recognized that aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) are associated with risk of upper gastrointestinal (the stomach) bleeding. It is increasingly recognized to have adverse effects in the small bowel, including ulcers resulting in bleeding. Bleeding from the small bowel has been very difficult to diagnose as it is beyond the reach of the conventional endoscopy. But with advances in endoscopic technique, video capsule endoscopy is now available to visualize the whole of the digestive tract. Capsule endoscopy is the size and shape of a pill which contains a tiny camera. After ingesting the capsule, pictures are taken inside of the gastrointestinal tract. Capsule endoscopy is now recommended to be a noninvasive test to identify source of small bowel bleeding. Investigators have recently shown that misoprostol can heal small bowel ulcers in aspirin users with small bowel bleeding. However, the complete healing rate with misoprostol alone was only 40%. This suggests that we should continue to investigate for additional therapies in order to achieve higher success rate of healing of aspirin-induced small bowel ulcers. Rifaximin is a non-absorbed oral antibiotic that targets the gastrointestinal tract. It was first described in 1982 and introduced into the Italian market 5 years later. Since then, rifaximin has had U.S. Food and Drug Administration (FDA) approval for treatment of travellers' diarrhea (year approved = 2004), hepatic encephalopathy (year approved=2010), irritable bowel syndrome (IBS) with diarrhea (year approved= 2015). Unlike the systematically available antibiotics, it allows localized enteric targeting of pathogens and is associated with minimal risk of systemic toxicity or side effects. In addition, the restricted use of non-absorbed oral antibiotics should also reduce the development of wide spread resistance. The aim of this study is to test the hypothesis that the combination therapy of rifaximin and misoprostol is superior to misoprostol alone for healing of small bowel ulcers in aspirin users complicated by small bowel bleeding. Participants are invited to this study because some predefined lesions are detected by the small bowel capsule endoscopy. Participants will be randomly assigned to receive either a combination therapy of misoprostol and rifaximin or misoprostol and rifaximin placebo for 8 weeks. Participants will be contacted by telephone after 1 week for any adverse events. Participants will then return at Week 8 to undergo a follow-up capsule endoscopy. Lab tests, drug compliance, and adverse events will be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Small Bowel Disease, Rifaximin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
78 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rifaximin
Arm Type
Active Comparator
Arm Description
ASA daily + misoprostol + Rifaximin (Rifaximin group)
Arm Title
Rifaximin Placebo
Arm Type
Placebo Comparator
Arm Description
ASA daily + misoprostol + Placebo Rifaximin (Placebo group)
Intervention Type
Drug
Intervention Name(s)
Rifaximin
Intervention Description
Rifaximin 200mcg four times daily
Intervention Type
Drug
Intervention Name(s)
Placebo oral tablet
Intervention Description
Placebo Rifaximin four times daily
Primary Outcome Measure Information:
Title
Healing of small bowel ulcers
Description
Capsule endoscopy will be performed to check if there is complete healing of small bowel ulcers, with or without red spots.
Time Frame
8 weeks after randomization
Secondary Outcome Measure Information:
Title
Change in numbers of ulcer/erosions
Description
Change in numbers of ulcer/erosions from baseline within and between groups
Time Frame
8 weeks after randomization
Title
Change in blood hemoglobin level
Description
Change in blood hemoglobin level from baseline within and between groups
Time Frame
8 weeks after randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Suspected small bowel overt bleeding - melena or hematochezia with or without a source of bleeding from gastroscopy and colonoscopy or suspected small bowel occult blood loss - defined as a significant decrease in hemoglobin (> 2g/dL), without a source of bleeding from gastroscopy 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) Continuous use of aspirin for the duration of the trial Age ≥ 18 Written informed consent obtained Exclusion Criteria: Increased risk of capsule retention (e.g. gastric outlet obstruction, bypass surgery, Crohn's disease or suspected small bowel stricture) Abnormal findings on gastroscopy that may account for bleeding episode: clean-based ulcer >2 cm or >5 erosions, esophageal varices, grade C or D erosive esophagitis, vascular malformations Unable to swallow the capsule endoscopy Terminal illness Concomitant use of NSAIDs, sucralfate, rebamepide, antibiotics, corticosteroids (prednisolone >7.5 mg daily or equivalent), and iron supplement Pregnancy (except LMP within 7 days) or women of child-bearing age without regular use of contraception Contraindications to colonoscopy or capsule endoscopy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jessica CHING, MPH
Phone
+852 3505 3524
Email
jessicaching@cuhk.edu.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Pui Kuan Cheong, MPH
Phone
+852 3505 3476
Email
jcheong@cuhk.edu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francis Chan, MD
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing Friendship Hospital, Capital Medical University
City
Beijing
State/Province
Beijing
ZIP/Postal Code
000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rui Cheng, MD
Phone
86-15901103303
Email
15901103303@163.com
Facility Name
Prince of Wales Hospital
City
Hong Kong
ZIP/Postal Code
000
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pui Kuan Cheong, MPH
Phone
852-35053476
Email
jcheong@cuhk.edu.hk

12. IPD Sharing Statement

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Rifaximin and Misoprostol Combination Therapy for Healing of Small Bowel Ulcers in Aspirin Users

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