Haemorrhage Alleviation With Tranexamic Acid- Intestinal System (HALT-IT)
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01658124|
Recruitment Status : Recruiting
First Posted : August 6, 2012
Last Update Posted : December 2, 2017
|Condition or disease||Intervention/treatment||Phase|
|Gastrointestinal Bleeding||Drug: Tranexamic Acid Drug: Placebo||Phase 3|
Hide Detailed Description
BACKGROUND: Acute gastrointestinal (GI) haemorrhage is one of the most common gastrointestinal emergencies. It is an important cause of mortality and morbidity in high, middle and low income countries. The most common causes of upper GI haemorrhage are peptic ulcer, oesophageal varices and erosive mucosal disease, although the relative frequency of the different causes varies in different countries. Acute upper GI haemorrhage accounts for around 50,000 hospital admissions each year in the UK and has a case fatality of about 10%. The incidence is highest among the most disadvantaged social groups. Lower GI haemorrhage accounts for a further 15,000 hospital admissions each year and has a case fatality of between 10% and 20%. Upper GI haemorrhage is also a common medical emergency in low and middle income countries. Patients are usually young and poor and the source of bleeding is more often oesophageal varices. Fibrinolysis may play an important pathological role in GI haemorrhage due to premature breakdown of haemostatic plugs at sites of mucosal injury. Tranexamic acid (TXA) is a synthetic derivative of the amino acid lysine which inhibits fibrinolysis by blocking the lysine binding sites on plasminogen. It is a widely used treatment with a known safety profile. There is reliable evidence that TXA reduces blood transfusion in surgical patients. A systematic review including 65 trials shows that TXA reduces the probability of blood transfusion by 39% (RR=0.61, 95% CI 0.53 to 0.70) compared to control. The effect of TXA on the risk of thromboembolic events in surgical patients remains uncertain, although there is no evidence of any increase in risk. The CRASH-2 trial showed that administration of TXA significantly reduces deaths due to bleeding (RR=0.85, 95% CI 0.76 to 0.96), and all-cause mortality (RR=0.91, 95% CI 0.85 to 0.97) in trauma patients with significant extra-cranial bleeding, with no increase in vascular occlusive events. A systematic review conducted by the investigators of TXA in GI bleeding identified nine randomised trials including a total of 1721 patients. Although there was a statistically significant reduction in the risk of death in patients treated with TXA (RR=0.66, 95% CI 0.47 to 0.93), the estimate is imprecise and the overall quality of trials was poor. Furthermore, all but three of the trials were conducted before the widespread use of therapeutic endoscopy and proton pump inhibitors and even in aggregate the trials were too small to assess the effects of TXA on other clinical important outcomes such as thromboembolic events. For these reasons, the effectiveness and safety of TXA for GI haemorrhage is uncertain and there are currently no formal recommendations for its use as a treatment for GI bleeding.
AIM: The HALT-IT trial will determine the effect of TXA on mortality, morbidity (re-bleeding, non-fatal vascular events), blood transfusion, surgical intervention and health status in patients with acute gastrointestinal haemorrhage.
PRIMARY OUTCOME: The primary outcome is death in hospital within 28 days of randomisation (cause-specific mortality will also be recorded).
- Need for salvage surgery or radiological intervention
- Blood transfusion - blood or blood component units transfused
- Thromboembolic events (myocardial infarction, stroke, pulmonary embolism, deep vein thrombosis)
- Other adverse medical events (including renal failure, significant cardiac event, respiratory failure, hepatic failure, sepsis, pneumonia, seizure)
- Functional status measured using the Katz Index of Independence in Activities of Daily Living
- Time spent at an intensive care unit
- Length of stay in hospital
- Patient status (death, hospital readmission) at 12 months will be ascertained if appropriate databases are available in the recruiting country
A pragmatic, randomised, double blind, placebo controlled trial among 8,000 patients with clinically significant gastrointestinal bleeding
DIAGNOSIS AND INCLUSION/EXCLUSION CRITERIA:
Adults with acute significant upper or lower gastrointestinal bleeding. The diagnosis of significant bleeding is clinical but may include patients with hypotension, tachycardia, or those likely to need transfusion, urgent endoscopy or surgery. The fundamental eligibility criterion is the responsible clinician's 'uncertainty' as to whether or not to use tranexamic acid in a particular patient with gastrointestinal bleeding. If the clinician believes there is a clear indication for, or clear contraindication to, tranexamic acid use, the particular patient should not be randomised. There are no other pre-specified exclusion criteria.
TEST PRODUCT, REFERENCE THERAPY, DOSE AND MODE OF ADMINISTRATION:
A loading dose of tranexamic acid (1 gram by intravenous injection) or placebo (sodium chloride 0.9%) will be given as soon as possible after randomisation followed by an intravenous infusion of 3 grams over 24 hours or placebo (sodium chloride 0.9%).
This trial will be coordinated from the London School of Hygiene & Tropical Medicine Clinical Trials Unit (University of London) and conducted in hospitals in low, middle and high income countries.
DURATION OF TREATMENT AND PARTICIPATION:
The first dose will be given immediately after randomisation and the maintenance dose will be given immediately after the loading dose over 24 hours. Participation will end at discharge from randomising hospital, death or at 28 days post randomisation whichever occurs first.
CRITERIA FOR EVALUATION:
All patients randomly assigned to one of the treatments will be analysed together (regardless of whether or not they completed or received that treatment) on an intention to treat basis.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||12000 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||Tranexamic Acid for the Treatment of Gastrointestinal Haemorrhage: an International Randomised, Double Blind Placebo Controlled Trial|
|Study Start Date :||January 2013|
|Estimated Primary Completion Date :||June 2019|
|Estimated Study Completion Date :||September 2020|
Experimental: Tranexamic acid
(total dose 8 grams)
|Drug: Tranexamic Acid|
Placebo Comparator: Placebo
(Sodium Chloride 0.9%)
- The primary outcome is death in hospital (cause-specific mortality will also be recorded - haemorrhage, myocardial infarction, stroke, pulmonary embolism, pneumonia, malignancy, other) [ Time Frame: within 28 days of randomisation ]
- Re-bleeding [ Time Frame: within 28 days of randomisation ]
- Need for salvage surgery or radiological intervention [ Time Frame: within 28 days of randomisation ]
- Blood transfusion - blood or blood component units transfused [ Time Frame: within 28 days of randomisation ]
- Thromboembolic events (myocardial infarction, stroke, pulmonary embolism, deep vein thrombosis) [ Time Frame: within 28 days of randomisation ]
- Other adverse medical events (including renal failure, significant cardiac event, respiratory failure, hepatic failure, sepsis, pneumonia, seizure) [ Time Frame: within 28 days of randomisation ]
- Functional status measured using the Katz Index of Independence in Activities of Daily Living [ Time Frame: within 28 days of randomisation ]
- Time spent at an intensive care unit [ Time Frame: within 28 days of randomisation ]
- Length of stay in hospital [ Time Frame: within 28 days of randomisation ]
- Patient status (death, hospital readmission) [ Time Frame: within 12 months of randomisation ]Limited to recruiting countries with appropriate databases
- Death from haemorrhage [ Time Frame: within 28 days of randomisation ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01658124
|Contact: Haleema Shakur||++44(0)20 7958 firstname.lastname@example.org|
|Over 50 countries Worldwide||Recruiting|
|London, United Kingdom|
|Principal Investigator: Tim Harris, MD|
|Study Director:||Haleema Shakur||LSHTM|