Gastrointestinal Hemorrhage Clinical Trial
Official title:
A Comparison of Early Deployment of a Video Capsule (Endocapsule EC-10: Olympus Tokyo. Japan) in the Emergency Department Versus Standard of Care Workup of Non-hematemesis Gastrointestinal Bleeding
The objectives of this study are to test whether there are statistically significant differences between the standard of care workup workup of non-hematemesis gastrointestinal bleeding by endoscopy [upper, lower and other tests], compared with deployment of a video capsule as the first test followed by the most appropriate endoscopic procedure based on video capsule findings, if needed. The investigators propose to examine differences in time to diagnosis, reduction in numbers of procedures, and length of stay between a standard of care workup protocol and our proposed protocol of early capsule endoscopy deployment.
After 40 years of considering gastrointestinal bleeding as upper or lower and largely
ignoring the small intestine, there is accumulating evidence that the standard of care
approach to the assessment of non-hematemesis gastrointestinal bleeding could be improved by
early deployment of a video capsule (VCE) as the first diagnostic test. Currently, VCE is
considered the gold standard as the diagnostic test for small intestinal bleeding. In a
recent study at the University of Massachusetts (UMass) 336 patients who presented to the
emergency department (ED) with complaints of gastrointestinal bleeding 36 patients (10.7%)
were given a VCE during their stay.
In patients with hematemesis, upper endoscopy remains the diagnostic and therapeutic modality
of choice. However patients with melena and hematochezia may benefit from early VCE since
both signs and symptoms provide poor localization as to the origin of bleeding. Data from
this previous Umass study suggests that the ingestion of a VCE in the ED could quickly and
non-invasively provide clinicians accurate data as to the origin of the bleeding. This
information could provide a guide to further management of the patient. VCE is able to
visualize bleeding in the esophagus, stomach, duodenum, small intestine and right colon,
thereby eliminating the guess work of deciding which endoscopic approach to use.
At UMass, that same study showed that of the 36 patients who received a video capsule, 26
(72.2%) had diagnostic studies (i.e. bleeding was identified). In comparison, 152 patients
required upper endoscopy (of which 52.9% were diagnostic) and 64 patients required
colonoscopy (of which 47% were diagnostic). Of those 26 patients with diagnostic capsule
studies, 13 also required upper endoscopy, 1 required a colonoscopy, and 4 required both a
colonoscopy and endoscopy. It is important to recognize, however, that often capsule studies
are performed after upper endoscopy and colonoscopy and performed and are found to be
negative. This sequence is the standard of care work up of bleeding. Despite being performed
later in the hospital course of our patients, capsule studies have a high diagnostic yield.
In reality VCE is used uncommonly in acute bleeding because it is rarely considered in the
context of acute GI bleeding In this study, the investigators propose the approach of using
the video capsule as the first diagnostic test prior to colonoscopy and endoscopy; this may
lead to a shortened time to diagnosis, a reduction in length of stay, and a reduction in
numbers of procedures due to early, accurate localization of the source of bleeding. All of
these components could result in better quality of care and cost containment. Further, it is
known that 80% of patients stop bleeding spontaneously. Thus the earlier they are examined
the more likely the origin of the bleeding is likely to be found The use of VCE has been
approved by the FDA since 2001 for small intestinal bleeding obscure GI Bleeding. It is very
safe and no deaths associated with its use have been reported. More than two million capsules
have been used and complications of obstruction and perforation are extremely rare.
Interest in the broader use of VCE is accumulating. More recently studies of VCE deployed in
the ED, in patients with upper GI bleeding showed improved management. Our group recently
demonstrated that the closer a VCE is performed to the time of bleeding the higher the
likelihood of locating the sources and the higher the therapeutic intervention rate. The
investigators also have demonstrated that the use of capsule endoscopy in patients with
non-hematemesis gastrointestinal bleeding (NHGIB) has a higher diagnostic yield than does
colonoscopy. With improved diagnostic yields, capsule endoscopy may help clinicians by
providing guidance in the management of patients with NHGIB.
This protocol is be the first attempt to prospectively examine this concept in a large
randomized prospective trial. The questions the investigators are studying are: can early
capsule intervention decrease time to diagnosis, numbers of procedures and hospital length of
stay in patients with non-hematemesis gastrointestinal bleeding?
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02903017 -
Local Administration of Tranexamic Acid in Upper Gastrointestinal Hemorrhage
|
Phase 4 | |
Recruiting |
NCT02514304 -
Study of the Risk Factors and Outcomes After Gastrointestinal Bleeding
|
||
Completed |
NCT02384122 -
Efficacy of Octreotide on Blood and Iron Requirements in Patients With Anemia Due to Angiodysplasias
|
Phase 3 | |
Completed |
NCT01477320 -
Enteral Nutrition as Stress Ulcer Prophylaxis in Critically Ill Patients.
|
N/A | |
Not yet recruiting |
NCT01549418 -
The Risk of Bleeding After Removal of Large Colorectal Polyps in Patients Taking Aspirin
|
Phase 4 | |
Completed |
NCT02105532 -
Transfusion in Gastrointestinal Bleeding
|
Phase 2/Phase 3 | |
Recruiting |
NCT05226221 -
Gastrointestinal Emergency Surgery: Evaluation of Morbidity and Mortality
|
||
Active, not recruiting |
NCT02874326 -
Octreotide in Patients With GI Bleeding Due to Rendu-Osler-Weber
|
Phase 2 | |
Completed |
NCT02928939 -
Therapeutic Conflicts and Multimorbidity
|
||
Withdrawn |
NCT01215058 -
Gastroprotective Agent Compliance in Patients at Risk Suffering From a Gastrointestinal(GI) Ulcer
|
N/A | |
Completed |
NCT01029626 -
Glasgow-Blatschford Score Validation in Digestive Hemorrhage
|
N/A | |
Completed |
NCT00251979 -
A Study to Prevent Rebleeding After Initial Successful Primary Endoscopic Haemostasis of a Bleeding Peptic Ulcer
|
Phase 3 | |
Completed |
NCT02991612 -
Rifaximin in Patients With Gastroesophageal Variceal Bleeding
|
N/A | |
Recruiting |
NCT02964195 -
Efficacy of Rifaximin in Treatment of Cirrhotic Gastroesophageal Variceal Bleeding
|
N/A | |
Terminated |
NCT02609100 -
Video Capsule Endoscopy Versus Colonoscopy in Patients With Melena and Negative Upper Endoscopy
|
N/A | |
Completed |
NCT02965209 -
European Novel Motorized Spiral Endoscopy Trial
|
N/A | |
Completed |
NCT02349490 -
Seraseal for Endoscopic Hemostasis
|
Phase 4 | |
Completed |
NCT01872286 -
Comparison of the Frequency-altering AKE-1 Capsule and Pillcam SB2
|
N/A | |
Withdrawn |
NCT01005147 -
Effect of Tranexamic Acid in Upper Gastrointestinal Bleeding
|
N/A | |
Completed |
NCT00570973 -
Band Ligation Versus Transjugular Intrahepatic Portosystemic Stent Shunt (TIPS) in Cirrhotics With Recurrent Variceal Bleeding Non Responding to Medical Therapy
|
Phase 4 |