Ultra-early Tranexamic Acid After Subarachnoid Hemorrhage. (ULTRA)
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|ClinicalTrials.gov Identifier: NCT02684812|
Recruitment Status : Completed
First Posted : February 18, 2016
Last Update Posted : November 12, 2020
|Condition or disease||Intervention/treatment||Phase|
|Subarachnoid Hemorrhage||Drug: Tranexamic Acid||Phase 2 Phase 3|
Approximately 50% of all patients with a subarachnoid hemorrhage (SAH) die due to the hemorrhage or subsequent complications. There are several major causes for this course, such as in-hospital rebleed in 21.5% which most frequently occurs within the first 6 hours after the primary hemorrhage ("ultra-early rebleed"). A major part of the patients with a rebleed die during hospital admission and when they survive, they develop more severe cognitive dysfunctions. Reducing the rebleeds by ultra-early administration of tranexamic acid (TXA) could be a major factor in improving the functional outcome after SAH.
To evaluate whether SAH patients treated by state-of-the-art SAH management with additional ultra-early and short term TXA administration have a significantly higher percentage of favourable outcome after six months (score 0-3 on the Modified Rankin Scale) compared to the group treated by up-to-date SAH management without additional TXA.
To evaluate whether: 1) TXA reduces in-hospital rebleeds and case fatalities; 2) TXA causes more ischemic stroke 3) TXA causes more complications (such as thromboembolic events, hydrocephalus, extracranial thrombosis or hemorrhagic complications) during treatment, admission and follow-up; 4) there is a difference in causes of poor outcome between groups; 5) there is a difference in discharge locations between groups; 6) there is an association between the time between hemorrhage and TXA administration and outcome; 7) TXA increases (micro)infarctions after endovascular treatment; 8) TXA reduces health-care costs between discharge and six months after hemorrhage; 9) TXA improves quality of life at six months after hemorrhage; 10) there are differences in rebleed rates and outcome between genders or groups with different WFNS scores at admission.
Multicenter, prospective, randomized, open label treatment with blind endpoint assessment.
Adult patients (18 years and older) included within 24 hours after SAH. Group one: standard treatment with additional administration of 1 g TXA intravenously in ten minutes, immediately after the diagnosis SAH, succeeded by continuous infusion of 1 g per 8 hours until a maximum of 24 hours. Group two: standard treatment with no TXA administration. Both groups undergo a standardized and validated interview at discharge and six months after hemorrhage to assess the modified Rankin Scale score, and both groups receive a questionnaire to evaluate health-care costs and quality of life.
Primary: modified Rankin Scale score after six months, dichotomized into favourable and unfavourable outcome. Secondary: rebleed and case fatality rate, complications during the first six months after hemorrhage, (micro)infarctions at MR imaging after endovascular treatment, health-care costs from discharge until six months, quality of life at six months and differences in rebleed rates and outcome between genders or WFNS score at admission.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Subjects are randomly allocated to ultra-early TXA therapy or standard treatment. Complications are minor and the expected benefit is large compared with separate studies done with antifibrinolytic medications. In these studies, the safety of the use of these medications in this study population is confirmed. In this patient group there are adequate, disoriented and comatose patients on admission, so a part of the studied patients are incapacitated when undergoing the study. To extrapolate the conclusions of this study to clinical protocols it is necessary to include patients with a SAH in all different severity grades. Weighing carefully the benefits versus the burden and risks, it is assumed that patients will benefit from ultra-early TXA administration with minimal burden during therapy.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||955 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Masking Description:||PROBE Design|
|Official Title:||Ultra-early Tranexamic Acid After Subarachnoid Hemorrhage. A Prospective, Randomized, Multicenter Study.|
|Actual Study Start Date :||July 16, 2012|
|Actual Primary Completion Date :||July 29, 2019|
|Actual Study Completion Date :||November 1, 2020|
Active Comparator: Tranexamic Acid
Eligible subjects are randomly assigned to immediate administration of TXA (1 g i.v.) after a diagnosis of SAH, as confirmed by CT-scan of the brain, continued by continuous infusion of 1 g per 8 hours to a maximum of 24 hours after start of medication. A maximum of 4 g TXA (1 g bolus + 3x 1 g continuous infusion) can be administered to one patient.
Drug: Tranexamic Acid
Treatment until aneurysm treatment or maximum dosage of 4 gram
Other Name: Cyklokapron
No Intervention: Control
- Modified Rankin Scale (mRS) [ Time Frame: six months ]Good (mRS 0-3) and Poor (mRS 4-6)
- Date and cause of death [ Time Frame: Maximum six month ]Assessment of cause of death by a committee (intensive care/neurosurgeon)
- Cause of poor outcome [ Time Frame: six months ]Assessment of which events during hospital admission led to a poor outcome defined as mRS 4 and 5 by a committee (intensive care/neurosurgeon)
- Rebleed and time interval after first hemorrhage [ Time Frame: six months ]The time interval between the initial hemorrhage and occurence of a recurrent bleeding will be recorded.
- Thromboembolic events during endovascular treatment [ Time Frame: up to 48 hours ]Complications during endovascular treatment will be recorded (ie occurence of clotting in one of the vessels)
- Ischemic stroke (Dealyed cerebral ischemia) [ Time Frame: 14-20 days ]
- Extracranial thrombosis [ Time Frame: six months ]
- Hydrocephalus and treatment modality [ Time Frame: six months ]Occurence of a hydrocephalus will be recorded and which treatment modality is used to treat the hydrocephalus
- Hemorrhagic complications (intra- and extracranial) [ Time Frame: six months ]
- Time interval from last hemorrhage to first TXA administration [ Time Frame: 24 hours ]
- Discharge location [ Time Frame: six months ]
- Infarctions on MR imaging at six months after endovascular treatment [ Time Frame: six months ]
- Health-care costs between discharge and six months after hemorrhage [ Time Frame: three and six months ]Questionnaires
- Quality of life at six months after hemorrhage [ Time Frame: six months ]Questionnaire (EQ-5D)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02684812
|Academic Medical Centre|
|Principal Investigator:||William P Vandertop, PhD MD||Department of Neurosurgery|