Resolution Endoclips Vs Epinephrine Injection and Heater Probe
Primary Purpose
Peptic Ulcer Hemorrhage
Status
Terminated
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Resolution clip (endo-clipping device)
Sponsored by
About this trial
This is an interventional treatment trial for Peptic Ulcer Hemorrhage focused on measuring Bleeding Peptic Ulcer, Endoscopic treatment
Eligibility Criteria
Inclusion Criteria: Age >16 , can obtain written consent Ulcers that require endoscopic therapy with SRH: Forrest I a, Ib, II a and II b Exclusion Criteria: Moribund patients with terminal malignancy Pregnancy Intercurrent ulcer complication that prevents treatment and surgery becomes mandatory such as bulbar stenosis and ulcer perforation
Sites / Locations
- Endocopy Center, Prince of Wales Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
DUAL THERAPY
'Resolution clip
Arm Description
DUAL THERAPY
'Resolution clip
Outcomes
Primary Outcome Measures
Failure to control bleeding endoscopically and recurrent bleeding after initial control
linical rebleeding is defined by fresh hematemesis, fresh melena or hematochezia and signs of hypovolemic shock (systolic blood pressure of <90mmHg and pulse rate >110 per minute) and a drop in hemoglobin of > 2 g/dl per 24 hours despite adequate transfusion.
Rebleeding will be confirmed by an immediate endoscopy showing fresh blood in stomach or active bleeding from a previously seen ulcer. A clinical rebleeding will be independently reviewed by an adjudication panel.
Secondary Outcome Measures
Transfusion requirement (before and after endoscopic therapy)
Hospital stay
The need for surgery
Mortality from recurrent bleeding and all causes within 30 days of treatment
Treatment related complications e.g. perforation
Full Information
NCT ID
NCT00165009
First Posted
September 12, 2005
Last Updated
May 10, 2013
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT00165009
Brief Title
Resolution Endoclips Vs Epinephrine Injection and Heater Probe
Official Title
A Prospective Randomized Comparison of a Novel Hemostatic Clip (Resolution Clip™) to Combined Epinephrine Injection and Heater Probe Thermocoagulation in the Endoscopic Control of Ulcer Bleeding
Study Type
Interventional
2. Study Status
Record Verification Date
May 2013
Overall Recruitment Status
Terminated
Why Stopped
Slow recruitment
Study Start Date
June 2005 (undefined)
Primary Completion Date
January 2008 (Actual)
Study Completion Date
November 2008 (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
To compare the efficacy of a novel endoscopic clipping device(Resolution Clip™) and conventional epinephrine injection and heater probe thermocoagulation in control of peptic ulcer bleeding and prevention of recurrent bleeding
Detailed Description
The mortality of peptic ulcer bleeding remains high despite advances in endoscopy and medical therapy. Endoscopic therapy effectively controls peptic ulcer bleeding and substantially reduces recurrent bleeding. However, the best endoscopic therapy is still unclear. The current standard of therapy is injection with diluted epinephrine and heater probe (3.2mm) thermo-coagulation. However, it may be associated with complications such as precipitation of myocardial ischemia or heater probe perforation.
Endoscopic clipping is an emerging modality of endoscopic treatment, it mimics the use of surgical ligature on bleeding artery. Endo-clipping has the theoretical advantage over injection and heater probe in that the tissue reaction or damage will be much milder.
Resolution Clip™ is a newly developed endo-clipping device. It is superior to older generations of endo-clips in that it allows repeated closures and re-opening of clip so as to facilitate accurate deployment onto bleeding artery to ensure its optimal placement for hemostasis.
Consecutive patients with endoscopically confirmed bleeding peptic ulcer will be invited to participate in this double-blind, randomised trial, which compares the efficacy of Resolution clip and conventional dual endoscopic therapy. Patients will be compared for 30-day treatment failure rate.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peptic Ulcer Hemorrhage
Keywords
Bleeding Peptic Ulcer, Endoscopic treatment
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
103 (Actual)
8. Arms, Groups, and Interventions
Arm Title
DUAL THERAPY
Arm Type
No Intervention
Arm Description
DUAL THERAPY
Arm Title
'Resolution clip
Arm Type
Experimental
Arm Description
'Resolution clip
Intervention Type
Device
Intervention Name(s)
Resolution clip (endo-clipping device)
Intervention Description
Resolution clip (endo-clipping device)
Primary Outcome Measure Information:
Title
Failure to control bleeding endoscopically and recurrent bleeding after initial control
Description
linical rebleeding is defined by fresh hematemesis, fresh melena or hematochezia and signs of hypovolemic shock (systolic blood pressure of <90mmHg and pulse rate >110 per minute) and a drop in hemoglobin of > 2 g/dl per 24 hours despite adequate transfusion.
Rebleeding will be confirmed by an immediate endoscopy showing fresh blood in stomach or active bleeding from a previously seen ulcer. A clinical rebleeding will be independently reviewed by an adjudication panel.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Transfusion requirement (before and after endoscopic therapy)
Time Frame
within 30 days of therapy
Title
Hospital stay
Time Frame
within 30 days of therapy
Title
The need for surgery
Time Frame
within 30 days of therapy
Title
Mortality from recurrent bleeding and all causes within 30 days of treatment
Time Frame
within 30 days of therapy
Title
Treatment related complications e.g. perforation
Time Frame
within 30 days of therapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age >16 , can obtain written consent
Ulcers that require endoscopic therapy with SRH: Forrest I a, Ib, II a and II b
Exclusion Criteria:
Moribund patients with terminal malignancy
Pregnancy
Intercurrent ulcer complication that prevents treatment and surgery becomes mandatory such as bulbar stenosis and ulcer perforation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Justin C Wu, MD
Organizational Affiliation
Endoscopy Center, Prince of Wales Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Endocopy Center, Prince of Wales Hospital
City
Hong Kong SAR
Country
China
12. IPD Sharing Statement
Learn more about this trial
Resolution Endoclips Vs Epinephrine Injection and Heater Probe
We'll reach out to this number within 24 hrs