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To Compare a Hemostatic Powder TC-325 and Standard Treatment in the Control of Acute Upper Gastrointestinal Bleeding From Nonvariceal Causes (TC325)

Primary Purpose

Acute Upper Gastrointestinal Bleeding

Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Endoscopic Application of a Hemostatic Powder TC-325
Hemo-clipping
Epinephrine
thermo-coagulation
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Upper Gastrointestinal Bleeding

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with overt signs of upper gastrointestinal bleeding (hematemesis, melena and/or circulatory instability)
  • documented bleeding (Forrest I) from a non-variceal upper gastrointestinal source (gastro-duodenal ulcers, Mallory Weiss tear, cancers, Dieulafoy's and other vascular lesions) at endoscopy.

Exclusion Criteria:

  • without a full informed consent from the patient or his next of kin
  • Age <18 years
  • Pregnant
  • Lactating women

Sites / Locations

  • Endoscopy Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

TC-325

standard treatment

Arm Description

Endoscopic Application of a Hemostatic Powder TC-325, <=150gm , once

standard treatment of either hemo-clipping or thermo-coagulation with or without pre injection with diluted epinephrine <=20 clip or4 pulse , once only

Outcomes

Primary Outcome Measures

number of participants who presents and confirmed endoscopically as recurrent upper gastro-intestinal bleeding
( Further bleeding is defined by failure to control bleeding at index endoscopy, renewed hematemesis, fresh melena with circulatory instability after initial control of bleeding (systolic blood pressure of 90 mmHg or less or pulse rate of 110 per minute or more) and/or a drop in haemoglobin by 2 g/dl and haematocrit by 10% over 24 hours despite adequate transfusion. Further bleeding after initial endoscopic hemostasis requires documentation with immediate endoscopy which finds fresh blood and active bleeding from a previously treated upper GIB source. Patients with further bleeding after initial endoscopic control are considered to have reached an outcome endpoint.

Secondary Outcome Measures

number of participants who required subsequent endoscopic treatment upon recurrent bleeding
number of participants who required subsequent endoscopic treatment upon recurrent bleeding
number of participants who required subsequent surgical treatment upon recurrent bleeding
number of participants who required subsequent surgical treatment upon recurrent bleeding
number of participants who required further blood transfusion post randomization
number of participants who required further blood transfusion post randomization
Days of hospitalization post randomization
Days of hospitalization post randomization
number of days which participant required caring in Intensive care unit post randomization
number of days which participant required caring in Intensive care unit post randomization
number of participants with adverse events as a Measure of Safety and Tolerability (related or unrelated to endoscopic treatment)
number of participants with adverse events as a Measure of Safety and Tolerability (related or unrelated to endoscopic treatment
number of participants with mortality from all causes within 30 days randomization.
number of participants with mortality from all causes within 30 days randomization
Ease of endoscopic treatment as measured by Visual Analog Scale reported by Endoscopist
self reported VAS scale: 0 cm to 10 cm
procedure time of endoscopic treatment
procedure time of endoscopic treatment
number of participant who need extra assistant to accomplish the endoscopic treatment
number of participant who need extra assistant eg advanced endoscopist to accomplish the endoscopic treatment other than the main endoscopist

Full Information

First Posted
August 6, 2015
Last Updated
October 10, 2019
Sponsor
Chinese University of Hong Kong
Collaborators
North District Hospital, King Chulalongkorn Memorial Hospital, Changi General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02534571
Brief Title
To Compare a Hemostatic Powder TC-325 and Standard Treatment in the Control of Acute Upper Gastrointestinal Bleeding From Nonvariceal Causes
Acronym
TC325
Official Title
Endoscopic Application of a Hemostatic Powder TC-325 Versus Standard Treatment in the Control of Acute Upper Gastrointestinal Bleeding From Nonvariceal Causes; A Non-inferiority Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
September 7, 2015 (Actual)
Primary Completion Date
January 14, 2019 (Actual)
Study Completion Date
April 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
Collaborators
North District Hospital, King Chulalongkorn Memorial Hospital, Changi General Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Acute upper gastrointestinal bleeding is a common medical emergency. Bleeding peptic ulcers and other non-variceal causes constitute to about 95% of all cases of bleeding. Endoscopic treatment stops active bleeding, reduces rate of further bleeding and leads to improved patients outcomes. Endoscopic treatment can be technically demanding especially with lesions in difficult anatomic positions and to endoscopists with less experience. TC-325 is a propriety mineral blend hemostatic powder used to compress external civilian and military traumatic injuries. Investigators reported the first endoscopic application of TC-325 in 20 patients with actively bleeding gastro-duodenal ulcers. Investigators were able to stop bleeding in 19 of them. Subsequent case series from others reported a similar rate in the acute control of bleeding. To further define the role of TC-325 as a mono-therapy, a comparison to the current standard in endoscopic treatment is required. A non-inferiority randomized trial is being proposed to compare endoscopic use of TC-325 as a mono-therapy to current standards (i.e. hemoclips or thermo-coagulation with or without pre-injection with diluted epinephrine) in hemostatic treatment in patients with acute upper gastrointestinal bleeding from non-variceal causes. The non-inferiority primary endpoint is control of bleeding over 30 days from randomization. Other outcome endpoints include further endoscopic, angiographic or surgical treatments, hospitalization, blood transfusion and mortality. Investigators also compare ease of therapy measured by procedure time and a 10 cm visual analogue scale rated by endoscopists. Endoscopic application of TC-325 is a simple and less skill dependent technique. It may prove useful in bleeding from anatomically challenging sites of the gastro-duodenal tract.
Detailed Description
Impact and Objectives Long-term impact :Acute upper gastrointestinal bleeding is a common medical emergency. The majority of causes are non-variceal in etiology and are mostly peptic ulcers. Endoscopic treatment reduces further bleeding, surgery and deaths from the condition. The current endoscopic treatment to non-variceal causes includes.the use of hemo-clips and thermo-coagulation. Endoscopic treatment is skill demanding and can be challenging in difficult access areas in the gastroduodenal tract e.g. posterior bulbar duodenum. Endoscopic application of hemostatic powder (labeled TC-325) is technically easy. The proposed randomized trial is the first to compare TC-325 to standard treatment. An non-inferior treatment of hemostatic powder TC-325 would mean wider application of endoscopic treatment as most endoscopists are able to use it. It can at least be used for acute control of bleeding allowing time for more definitive treatment. Objectives : To compare clinical efficacy of the hemostatic powder TC-325 to standard treatment in overall rate of hemostasis in patients with active bleeding from a non-variceal source in the upper gastrointestinal tract. Investigators aim to determine the initial rate of hemostasis and the rate of further bleeding after initial control in both groups. Investigators would like to define role of TC-325 as a mono-therapy when compared to standard treatment. The rate of further bleeding after initial control would also inform us if endoscopic application of TC-325 should be followed by a second look endoscopy with targeted treatment to the bleeding artery. To compare ease of application of hemostatic powder TC-325 to standard treatment. Background of Research, Research Plan and Methodology : a. Background of research Acute upper gastrointestinal bleeding (AUGIB) is one of the commonest medical emergencies. Mortality in patients with AUGIB remains high. In the National United Kingdom Audit of 2007, the crude overall in patient mortality was 10%. Mortality increases in patients with advanced age and significant comorbid illnesses. Endoscopic therapy greatly improves outcomes in patients with AUGIB. In pooled analyses of randomized controlled trials on endoscopic therapy in patients with nonvariceal upper gastrointestinal bleeding, endoscopic therapy significantly reduces not only further bleeding but also surgery and deaths. The National United Kingdom audit in 2007 found continuing delays in endoscopy and treatment in patients admitted with AUGIB. Only 55% of patients judged to belong to the high risk group underwent endoscopy within 24 hours of their admissions, and only 74% of high risk lesions were offered endoscopic treatment. The gap in service provision may be an organization issue. The lack of skills in endoscopic therapy may also contribute to this shortfall. An easy-to-use endoscopic treatment is likely to help generalize endoscopic hemostasis. The current standard of endoscopic therapy consists of the use of hemoclips or thermo-coagulation with or without pre-injection with diluted epinephrine. TC-325 is a proprietary, inert inorganic mineral blend powder approved by FDA for the purpose of hemostasis. In the United States the powder is used for compression treatment of bleeding from external injuries in both civilian and combat casualties. The powder is highly absorbent. When in contact with fluid or blood the powder rapidly concentrates clotting factors at the bleeding site and forms an adherent coagulum. In 2011, Investigators reported the first endoscopic human application of the hemostatic powder TC-325. In 20 patients with Forrest type I bleeding from their gastro-duodenal ulcers, Investigators were able to control bleeding in 19 of them. The single patient with refractory bleeding from an angular gastric ulcer underwent angiography to his left gastric artery and a pseudo-aneurysm was found arising from the article. The aneurysm was successfully embolized with coils by angiographic methods. None of these patients needed surgery or died when followed up for 30 days. These initial results were encouraging. In gastroduodenal ulcers with Forrest I bleeding, rate of further bleeding would be around 55% if untreated by endoscopy. Subsequent to this pilot study, several series were published on the endoscopic use of TC-325. The pooled rate in the initial control of bleeding with the use of TC-325 was 89.6%. Rate of further bleeding after hemostasis was 19.2%. The reported series consisted of patients with different case-mix but exclusively non-variceal in etiologies. Indications for use of TC-325 also varied in these series. The powder was used as mono-therapy, in combination to other endoscopic therapies or as a rescue therapy when conventional endoscopic treatment failed. In the absence of comparative studies, the role of TC-325 remains undefined. Herein Investigators propose a randomized controlled study to compare endoscopic use of TC-325 as a mono-therapy to current standards of hemostasis using either hemo-clips or contact thermo-coagulation with or without diluted epinephrine in patients with active bleeding (Forrest type I) from non-variceal upper GI causes. Investigators hypothesize that endoscopic application of TC-325 would not be inferior in the control of bleeding from non-variceal sources when compared to standard treatment. If such is the case, endoscopic use of TC-325 may be preferred over existing techniques because of simplicity in TC-325 application. It appeals especially to endoscopists with less experience in endoscopic hemostasis. In lesions of challenging anatomical positions e.g. posterior bulbar duodenum, TC-325 may prove superior.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Upper Gastrointestinal Bleeding

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
224 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TC-325
Arm Type
Experimental
Arm Description
Endoscopic Application of a Hemostatic Powder TC-325, <=150gm , once
Arm Title
standard treatment
Arm Type
Active Comparator
Arm Description
standard treatment of either hemo-clipping or thermo-coagulation with or without pre injection with diluted epinephrine <=20 clip or4 pulse , once only
Intervention Type
Device
Intervention Name(s)
Endoscopic Application of a Hemostatic Powder TC-325
Intervention Description
Endoscopic Application of a Hemostatic Powder TC-325 <=150g once
Intervention Type
Device
Intervention Name(s)
Hemo-clipping
Other Intervention Name(s)
quick clips
Intervention Description
Hemo-clipping <=20 clips
Intervention Type
Drug
Intervention Name(s)
Epinephrine
Other Intervention Name(s)
adrenaline
Intervention Description
epinephrine injection endoscopically <20 mls
Intervention Type
Device
Intervention Name(s)
thermo-coagulation
Other Intervention Name(s)
contact thermo-coagulation
Intervention Description
contact thermo-coagulation < = 4 pulses
Primary Outcome Measure Information:
Title
number of participants who presents and confirmed endoscopically as recurrent upper gastro-intestinal bleeding
Description
( Further bleeding is defined by failure to control bleeding at index endoscopy, renewed hematemesis, fresh melena with circulatory instability after initial control of bleeding (systolic blood pressure of 90 mmHg or less or pulse rate of 110 per minute or more) and/or a drop in haemoglobin by 2 g/dl and haematocrit by 10% over 24 hours despite adequate transfusion. Further bleeding after initial endoscopic hemostasis requires documentation with immediate endoscopy which finds fresh blood and active bleeding from a previously treated upper GIB source. Patients with further bleeding after initial endoscopic control are considered to have reached an outcome endpoint.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
number of participants who required subsequent endoscopic treatment upon recurrent bleeding
Description
number of participants who required subsequent endoscopic treatment upon recurrent bleeding
Time Frame
30 days
Title
number of participants who required subsequent surgical treatment upon recurrent bleeding
Description
number of participants who required subsequent surgical treatment upon recurrent bleeding
Time Frame
30 days
Title
number of participants who required further blood transfusion post randomization
Description
number of participants who required further blood transfusion post randomization
Time Frame
30 days
Title
Days of hospitalization post randomization
Description
Days of hospitalization post randomization
Time Frame
60 days
Title
number of days which participant required caring in Intensive care unit post randomization
Description
number of days which participant required caring in Intensive care unit post randomization
Time Frame
60 days
Title
number of participants with adverse events as a Measure of Safety and Tolerability (related or unrelated to endoscopic treatment)
Description
number of participants with adverse events as a Measure of Safety and Tolerability (related or unrelated to endoscopic treatment
Time Frame
30 days
Title
number of participants with mortality from all causes within 30 days randomization.
Description
number of participants with mortality from all causes within 30 days randomization
Time Frame
30 days
Title
Ease of endoscopic treatment as measured by Visual Analog Scale reported by Endoscopist
Description
self reported VAS scale: 0 cm to 10 cm
Time Frame
3 days
Title
procedure time of endoscopic treatment
Description
procedure time of endoscopic treatment
Time Frame
3 days
Title
number of participant who need extra assistant to accomplish the endoscopic treatment
Description
number of participant who need extra assistant eg advanced endoscopist to accomplish the endoscopic treatment other than the main endoscopist
Time Frame
3 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with overt signs of upper gastrointestinal bleeding (hematemesis, melena and/or circulatory instability) documented bleeding (Forrest I) from a non-variceal upper gastrointestinal source (gastro-duodenal ulcers, Mallory Weiss tear, cancers, Dieulafoy's and other vascular lesions) at endoscopy. Exclusion Criteria: without a full informed consent from the patient or his next of kin Age <18 years Pregnant Lactating women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
JAMES YW LAU, MD
Organizational Affiliation
CUHK
Official's Role
Principal Investigator
Facility Information:
Facility Name
Endoscopy Centre
City
Hong Kong
State/Province
Hong Kong
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34871051
Citation
Lau JYW, Pittayanon R, Kwek A, Tang RS, Chan H, Rerknimitr R, Lee J, Ang TL, Suen BY, Yu YY, Chan FKL, Sung JJY. Comparison of a Hemostatic Powder and Standard Treatment in the Control of Active Bleeding From Upper Nonvariceal Lesions : A Multicenter, Noninferiority, Randomized Trial. Ann Intern Med. 2022 Feb;175(2):171-178. doi: 10.7326/M21-0975. Epub 2021 Dec 7.
Results Reference
derived
PubMed Identifier
33929377
Citation
Laine L, Barkun AN, Saltzman JR, Martel M, Leontiadis GI. ACG Clinical Guideline: Upper Gastrointestinal and Ulcer Bleeding. Am J Gastroenterol. 2021 May 1;116(5):899-917. doi: 10.14309/ajg.0000000000001245. Erratum In: Am J Gastroenterol. 2021 Nov 1;116(11):2309.
Results Reference
derived

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To Compare a Hemostatic Powder TC-325 and Standard Treatment in the Control of Acute Upper Gastrointestinal Bleeding From Nonvariceal Causes

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