Evaluation the Performance of Given Diagnostic System in Detection of Bleeding Events in the Small Bowel
Primary Purpose
Gastrointestinal Hemorrhage
Status
Terminated
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Colon 2
Sponsored by
About this trial
This is an interventional diagnostic trial for Gastrointestinal Hemorrhage
Eligibility Criteria
Inclusion Criteria:
- Patients with overt GI bleeding (hematemesis, coffee-grounds, rectal bleeding and/or melena) with negative OGD but not critically ill, who should read positive on small bowel investigation (SBI)
- Patients with occult GI bleeding (Faecal occult blood test,FOBT +)
- Patients with suspected arteriovenous(AV) malformations.
- Patients treated with nonsteroidal antiinflammatory drugs (NSAIDs)
- Patients with active Crohn's disease(CD), with no evidence of obstruction
Exclusion Criteria:
- In patients with known or suspected gastrointestinal obstruction, strictures, or fistulas based on the clinical picture or pre-ingestion testing and profile.
- In patients with cardiac pacemakers or other implanted electromedical devices.
- In patients with dysphagia or other swallowing disorders.
- Unable to obtain informed written consent
Sites / Locations
- Prince of Wales Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Colon 2
Arm Description
using Colon 2 capsule in detecting bleeding events in small bowel
Outcomes
Primary Outcome Measures
Diagnostic yield for bleeding events in the small bowel
Review the capsule video to detect the bleeding events.
Secondary Outcome Measures
Full Information
NCT ID
NCT01441219
First Posted
August 2, 2011
Last Updated
March 4, 2013
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT01441219
Brief Title
Evaluation the Performance of Given Diagnostic System in Detection of Bleeding Events in the Small Bowel
Official Title
Evaluation the Performance of Given Diagnostic System in Detection of Bleeding Events in the Small Bowel: a Single-arm Prospective Cohort Study.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2013
Overall Recruitment Status
Terminated
Why Stopped
Results were obtained in another project.
Study Start Date
January 2011 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Obscure gastrointestinal bleeding (OGIB) has been one of the most challenging area in the field of gastroenterology, as small bowel is beyond the reach of ordinary endoscopes like oesophagogastroduodenoscopy (OGD) and colonoscopy. Thanks for the latest technological advancement for investigating small intestine, we are now capable of obtaining intraluminal images safely through capsule endoscopy (CE). Its role in obscure gastrointestinal bleeding, Crohn's disease and other small bowel pathologies has already been proven, and nowadays it is suggested by various authorities to be the first-line modality among all small bowel investigations.
The investigators group has showed that CE can alter the clinical management of patients with OGIB - patients with negative CE has lower rebleeding rate, and therefore we may adopt a conservative approach for them. Although supported by some other group as well, conflicting results were still reported in the literature about the out-come of these patients. The main criticisms for these studies are that, CE can only identify 61% of the underlying small bowel bleeding pathology, and one can never ascertain the outcome of patients with negative CE examination. Apparently there is still room for improvement in the current CE technology.
Detailed Description
Newer generation of CE (PillCam ColonTM) has been developed to investigate the large bowel. It is different from small bowel CE that it consists of two cameras at both ends of the capsule, so as to enhance the coverage of colonic mucosa visualization. An improved generation of this colon capsule, named PillCam Colon 2TM, is also in its developmental phase. With the new "adaptive frame rate" (AFR) technology, the CE optimizes the visual coverage of the bowel by increasing the frame rate up to 35 frames per second when the capsule is moving quickly in certain areas, while decreasing the frame rate down to 4 frames per second when the capsule is moving slowly or remains stationary so as to conserve the battery life. Preliminary data from colorectal cancer screening has shown that it could improve the diagnostic yield of colonic polyps.
The investigators hypothesize that, by re-programming the PillCam Colon 2TM so as to initiate AFR since ingestion, it could improve the visualization of small intestinal lumen and hence improves the sensitivity of small bowel CE examination.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastrointestinal Hemorrhage
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 2, Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Colon 2
Arm Type
Experimental
Arm Description
using Colon 2 capsule in detecting bleeding events in small bowel
Intervention Type
Device
Intervention Name(s)
Colon 2
Other Intervention Name(s)
C2
Intervention Description
Ingest one colon 2 capsule
Primary Outcome Measure Information:
Title
Diagnostic yield for bleeding events in the small bowel
Description
Review the capsule video to detect the bleeding events.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with overt GI bleeding (hematemesis, coffee-grounds, rectal bleeding and/or melena) with negative OGD but not critically ill, who should read positive on small bowel investigation (SBI)
Patients with occult GI bleeding (Faecal occult blood test,FOBT +)
Patients with suspected arteriovenous(AV) malformations.
Patients treated with nonsteroidal antiinflammatory drugs (NSAIDs)
Patients with active Crohn's disease(CD), with no evidence of obstruction
Exclusion Criteria:
In patients with known or suspected gastrointestinal obstruction, strictures, or fistulas based on the clinical picture or pre-ingestion testing and profile.
In patients with cardiac pacemakers or other implanted electromedical devices.
In patients with dysphagia or other swallowing disorders.
Unable to obtain informed written consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joseph JY Sung, MD
Organizational Affiliation
CUHK
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital
City
Hong Kong
Country
China
12. IPD Sharing Statement
Learn more about this trial
Evaluation the Performance of Given Diagnostic System in Detection of Bleeding Events in the Small Bowel
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