Tranexamic Acid for The Treatment of Gastrointestinal Bleeding
Primary Purpose
Gastrointestinal Bleeding
Status
Suspended
Phase
Not Applicable
Locations
Indonesia
Study Type
Interventional
Intervention
Tranexamic acid injection
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Gastrointestinal Bleeding focused on measuring Gastrointestinal bleeding, Tranexamic acid, Clinical trial
Eligibility Criteria
Inclusion Criteria:
- Adults
- Patients with acute lower and upper gastrointestinal bleeding (assessed clinically)
- Patients agreed to participate in the study and signed the informed consent
Exclusion Criteria:
- Allergy with tranexamic acid
- Patients considered by the clinician can not be randomized to participate in the study
- Patients with chronic kidney disease stage III - V
Sites / Locations
- Cipto Mangunkusumo National Central General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Tranexamic acid injection
Placebo
Arm Description
Group with tranexamic acid injection
Group with Placebo
Outcomes
Primary Outcome Measures
Re-bleeding
Total incidence number of re-bleeding
Secondary Outcome Measures
Number of death
Total number patients who die
Need for blood transfusion
Total number of patients with blood transfusion
Length of stay in intensive care unit
Average time of stay each participants in intensive care unit
Need for endoscopic hemostasis
Total number of patients with endoscopic hemostasis
Quality of life (physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health)
Short Form-36 Questionnaire includes one scale for each of eight measured health domains: physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health. All health domain scales are scored using norm-based scores ranging 0 to 100 with higher scores indicate better health
Level of anxiety
Hamilton Anxiety Rating Scale; Each item is scored of 0 (not present) to 4 (severe), with total score range of 0-56, where <14 indicates no anxiety, 14-20 mild anxiety, 21-27 moderate anxiety, 28-41 severe anxiety and 42-56 very severe anxiety
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03540368
Brief Title
Tranexamic Acid for The Treatment of Gastrointestinal Bleeding
Official Title
The Role of Tranexamic Acid for the Treatment of Gastrointestinal Bleeding: A Randomized Double-blind Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Suspended
Why Stopped
increased number of patients death
Study Start Date
July 4, 2018 (Actual)
Primary Completion Date
March 1, 2019 (Actual)
Study Completion Date
September 1, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Indonesia University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Studies showed that in cases of gastrointestinal bleeding, injection tranexamic acid decreasing the risk of death and the need of surgical intervention. However, the quality of most clinical trials were not good and the results were not significant. Injection tranexamic acid does not become one of the treatment option in the international guidelines nor in national consensus, so the effectiveness and the safety of its use in the treatment of gastrointestinal bleeding remains unclear and not routinely used.
In Indonesia, injection tranexamic acid in gastrointestinal bleeding is limitedly used and recorded. Therefore, a clinical trial study of injection tranexamic acid is required to assess the effectiveness and the safety in the treatment of gastrointestinal bleeding.
Detailed Description
This study is a randomized double-blind controlled trial study. Interventions were given in the form of tranexamic acid injection compared to placebo in patients with acute upper and lower gastrointestinal bleeding. Tranexamic acid were administered intravenously 1 gram loading dose, followed by 3 grams maintenance dose in infusion for 24 hours. Other routine and standardized drugs for gastrointestinal bleeding will still be given. Statistical analysis will use: Chi square test or Kolmogorov-Smirnov with alternative Fisher test for categorical dependent-variable; Independent T-Test with alternative Mann-Whitney test for two-group numerical dependent-variable; and one-way ANOVA with alternative Kruskal-Wallis for more than two-groups numerical dependent-variable.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastrointestinal Bleeding
Keywords
Gastrointestinal bleeding, Tranexamic acid, Clinical trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
All patients will receive standard treatment equally
Allocation
Randomized
Enrollment
336 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Tranexamic acid injection
Arm Type
Experimental
Arm Description
Group with tranexamic acid injection
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Group with Placebo
Intervention Type
Drug
Intervention Name(s)
Tranexamic acid injection
Intervention Description
Administering tranexamic acid loading dose 1 gram in 100 cc sodium chloride 0,9%, followed by maintenance dose 3 grams in infusion for 24 hours.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Administering placebo or sodium chloride 0,9% intravenously
Primary Outcome Measure Information:
Title
Re-bleeding
Description
Total incidence number of re-bleeding
Time Frame
30 days after randomisation
Secondary Outcome Measure Information:
Title
Number of death
Description
Total number patients who die
Time Frame
30 days after randomisation
Title
Need for blood transfusion
Description
Total number of patients with blood transfusion
Time Frame
30 days after randomisation
Title
Length of stay in intensive care unit
Description
Average time of stay each participants in intensive care unit
Time Frame
30 days after randomisation
Title
Need for endoscopic hemostasis
Description
Total number of patients with endoscopic hemostasis
Time Frame
30 days after randomisation
Title
Quality of life (physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health)
Description
Short Form-36 Questionnaire includes one scale for each of eight measured health domains: physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health. All health domain scales are scored using norm-based scores ranging 0 to 100 with higher scores indicate better health
Time Frame
30 days after randomisation
Title
Level of anxiety
Description
Hamilton Anxiety Rating Scale; Each item is scored of 0 (not present) to 4 (severe), with total score range of 0-56, where <14 indicates no anxiety, 14-20 mild anxiety, 21-27 moderate anxiety, 28-41 severe anxiety and 42-56 very severe anxiety
Time Frame
30 days after randomisation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adults
Patients with acute lower and upper gastrointestinal bleeding (assessed clinically)
Patients agreed to participate in the study and signed the informed consent
Exclusion Criteria:
Allergy with tranexamic acid
Patients considered by the clinician can not be randomized to participate in the study
Patients with chronic kidney disease stage III - V
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ari F Syam, Dr, MD
Organizational Affiliation
Gastroenterology Division, Internal Medicine Department RSCM/UI
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cipto Mangunkusumo National Central General Hospital
City
Jakarta Pusat
State/Province
DKI Jakarta
ZIP/Postal Code
10430
Country
Indonesia
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
25414987
Citation
Bennett C, Klingenberg SL, Langholz E, Gluud LL. Tranexamic acid for upper gastrointestinal bleeding. Cochrane Database Syst Rev. 2014 Nov 21;2014(11):CD006640. doi: 10.1002/14651858.CD006640.pub3.
Results Reference
background
Learn more about this trial
Tranexamic Acid for The Treatment of Gastrointestinal Bleeding
We'll reach out to this number within 24 hrs