Actively Recruiting
Tranexamic Acid to Prevent OpeRation in Chronic Subdural Hematoma
Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2024-06-20
554
Participants Needed
1
Research Sites
593 weeks
Total Duration
On this page
Sponsors
A
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead Sponsor
Z
ZonMw: The Netherlands Organisation for Health Research and Development
Collaborating Sponsor
AI-Summary
What this Trial Is About
Rationale: Chronic subdural hematoma (cSDH) is a frequently occurring disease, occurring mainly in the elderly. Surgical evacuation is effective, but also associated with life-threatening risks. In these old, often frail, patients with multi-comorbidity, surgery also comes with significant risks for future cognitive functioning and therefore, loss of independency. In five small retrospective series, tranexamic acid (TXA), an antifibrinolytic drug, showed a beneficial effect on the spontaneous resolution of the hematoma and, with that, the necessity for surgery. This randomised, placebo-controlled clinical trial aims to prove the efficacy of TXA. Objectives: Primarily to evaluate the efficacy of TXA to prevent surgery for cSDH. Secondarily to evaluate the efficacy of TXA to reduce cSDH volume, neurological impairment (mNIHSS), the incidence of falling incidents, the mortality rate, the use of care and health-related costs (iMCQ and iPCQ), to improve cognitive functioning (MOCA), performance in activities of daily living (Barthel and Lawton-Brody), functional outcome (mRS), the level of quality of life. Study design: Double-blind placebo-controlled multicentre randomized clinical trial. Study population: All patients, age 50 and above, diagnosed with cSDH for whom a conservative treatment is selected as primary treatment strategy. Intervention: The intervention group will receive oral TXA 500mg twice daily for 4 weeks, the control group will receive a placebo twice daily. The TXA or placebo treatment is additional to standard care. Main study endpoint: The number of patients requiring surgery within 12 weeks after start treatment. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients will use the study medication twice daily for four weeks. Follow-up is at 4, 8and 12 weeks with a standard CT-scan of the head, outpatient clinic visits and 4 patient-reported questionnaires. These outpatient clinic visits are standard care; the third CT-scan, the questionnaires and extra clinical tests are extra. Each patient may benefit from the study if the study medication proves effective in preventing surgery for cSDH, whereas the risk of potential side effects of the medication is slight (e.g. the risk of thromboembolic events is only 0.01-0.1%). Surgery remains a possibility for those patients in whom study medication is not effective.
CONDITIONS
Official Title
Tranexamic Acid to Prevent OpeRation in Chronic Subdural Hematoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Confirmed chronic subdural hematoma by CT scan
- Conservative treatment chosen as primary strategy based on clinical symptoms
- Glasgow Coma Scale score of 14 or higher
- Modified NIH Stroke Scale score of 4 or less
- Stable neurological condition with no new or worsening symptoms between neurologist and neurosurgeon assessments
You will not qualify if you...
- Immediate need for surgery due to severe symptoms such as uncontrollable headache, midline brain shift over 10mm, or expected death within 24 hours
- Structural causes of subdural bleeding like arachnoid cysts, vascular malformations, or recent (less than 1 year) brain surgery
- Aneurysmal subarachnoid hemorrhage
- Active treatment for deep vein thrombosis, pulmonary embolism, or cerebral thrombosis (excluding secondary prevention)
- Active blood clotting disorders or disseminated intravascular coagulation
- Known allergy to tranexamic acid or its components
- History of blood clotting disorders
- Severe kidney impairment (eGFR less than 30 ml/min or serum creatinine over 150 µmol/L)
- History of anemia with hemoglobin below 6 mmol/L
- History of seizures
- Difficulty swallowing oral medication safely
- Unable to provide informed consent or no legal representative available, including language barriers
AI-Screening
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Trial Site Locations
Total: 1 location
1
Academic Medical Center
Amsterdam, Netherlands, 1100DD
Actively Recruiting
Research Team
W
William P Vandertop, MD PhD
CONTACT
D
Dagmar Verbaan, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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