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Hemospray Versus the Combined Conventional Technique for Endoscopic Hemostasis of Bleeding Peptic Ulcers : A Pilot Study

Primary Purpose

Bleeding Peptic Ulcers

Status
Completed
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
Hemospray
Combined Conventional Technique
Sponsored by
Changi General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bleeding Peptic Ulcers

Eligibility Criteria

21 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Peptic ulcer with high-risk stigmata of recent hemorrhage (Forrest class IA, IB, IIA and IIB)

Exclusion Criteria:

  • Patients younger than 21 years of age
  • Refusal to participate in study
  • Contraindicated for endoscopy
  • Pregnant or lactating patients
  • Bleeding secondary to non-peptic ulcer source
  • Patients requiring mechanical ventilation
  • Patients with acute coronary syndrome

Sites / Locations

  • Changi General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Hemospray

Combined Conventional Technique

Arm Description

Hemospray (TC-325, Cook Medical Inc, Winston-Salem, NC, USA), an adsorptive nanopowder hemostatic agent

Standard dual therapy with saline adrenaline injection and hemoclip / heater probe application

Outcomes

Primary Outcome Measures

Re-bleeding Within 4 Weeks
drop in hemoglobin of at least 2 g/dl, associated with overt signs of GI bleed (melena, and/or hematemesis) fresh blood hematemesis melena with a hemodynamic instability (pulse rate > 100/min, systolic blood pressure < 90 mm Hg)

Secondary Outcome Measures

Initial Hemostasis Rate
Endoscopically verified cessation of bleeding for at least 5 minutes after treatment.

Full Information

First Posted
March 13, 2014
Last Updated
July 22, 2019
Sponsor
Changi General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02088385
Brief Title
Hemospray Versus the Combined Conventional Technique for Endoscopic Hemostasis of Bleeding Peptic Ulcers : A Pilot Study
Official Title
Pilot Study of a Randomized Controlled Trial Comparing Hemospray Versus the Combined Conventional Technique for Endoscopic Hemostasis of Bleeding Peptic Ulcers
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
November 2013 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Changi General Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Hemospray (TC-325, Cook Medical Inc, Winston-Salem, NC, USA), a new adsorptive nanopowder hemostatic agent for endoscopic treatment of high-risk bleeding peptic ulcers, provides significant ease of administration compared to the combined conventional technique of saline-adrenaline injection with mechanical clip or heater probe applications. The Hemospray powder is easily applied on ulcers at difficult endoscopic positions and ulcers with fibrotic bases, where the combined conventional technique has limited efficacy. Building up on preliminary work from small single-arm studies, the investigators aim to establish the efficacy and safety of Hemospray in treating bleeding peptic ulcers in comparison with the combined conventional technique. The investigators propose a pilot study to establish our centre's feasibility of performing a prospective, randomized, parallel group trial, which compares the efficacy of Hemospray with the combined conventional technique, in the endoscopic treatment of high-risk bleeding peptic ulcers. Patients with high-risk bleeding peptic ulcers will be treated with Hemospray to determine its initial hemostasis rate (defined as endoscopically verified cessation of bleeding for at least 5 minutes after endoscopic treatment), rebleeding rate (recurrent hemorrhage during a 4-week period following the initial hemostasis) and its safety profile.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bleeding Peptic Ulcers

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hemospray
Arm Type
Experimental
Arm Description
Hemospray (TC-325, Cook Medical Inc, Winston-Salem, NC, USA), an adsorptive nanopowder hemostatic agent
Arm Title
Combined Conventional Technique
Arm Type
Active Comparator
Arm Description
Standard dual therapy with saline adrenaline injection and hemoclip / heater probe application
Intervention Type
Device
Intervention Name(s)
Hemospray
Intervention Type
Device
Intervention Name(s)
Combined Conventional Technique
Primary Outcome Measure Information:
Title
Re-bleeding Within 4 Weeks
Description
drop in hemoglobin of at least 2 g/dl, associated with overt signs of GI bleed (melena, and/or hematemesis) fresh blood hematemesis melena with a hemodynamic instability (pulse rate > 100/min, systolic blood pressure < 90 mm Hg)
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Initial Hemostasis Rate
Description
Endoscopically verified cessation of bleeding for at least 5 minutes after treatment.
Time Frame
Within first endoscopy session

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Peptic ulcer with high-risk stigmata of recent hemorrhage (Forrest class IA, IB, IIA and IIB) Exclusion Criteria: Patients younger than 21 years of age Refusal to participate in study Contraindicated for endoscopy Pregnant or lactating patients Bleeding secondary to non-peptic ulcer source Patients requiring mechanical ventilation Patients with acute coronary syndrome
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew Kwek, MBBS
Organizational Affiliation
Changi General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Changi General Hospital
City
Singapore
Country
Singapore

12. IPD Sharing Statement

Learn more about this trial

Hemospray Versus the Combined Conventional Technique for Endoscopic Hemostasis of Bleeding Peptic Ulcers : A Pilot Study

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