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Study identifier: NCT06696079 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Restarting Early Versus Later Anticoagulation for Chronic Subdural Hematoma With Atrial Fibrillation

Condition: Chronic Subdural Hematoma · Atrial Fibrillation (AF)  ·  Sponsor: Rahul Raj

PhaseNA
Planned participants332
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this randomized clinical trial is to assess the benefit of early resumption versus late resumption of oral anticoagulation medication in adults with atrial fibrillation undergoing surgery for chronic subdural hematoma. The main questions it aims to answer are: * Does anticoagulation resumption 5 days after surgery as compared to 30 days after surgery result in fewer thromboembolic complications, without increasing the risk for bleeding? * Does anticoagulation resumption 5 days after surgery as compared to 30 days after surgery affect the risk of reoperation, functional outcome, mortality, and healthcare use? Researchers will compare early anticoagulation resumption (5 days) and late anticoagulation resumption (30 days) after chronic subdural hematoma surgery. Participants will either resume the medication 5 days or 30 days after the surgery. The participants will be followed up for 3 months after the surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Rahul Raj, MD, PhD  ·  +358504272516  ·  rahul.raj@hus.fi

Jarno Satopää, MD, PhD  ·  +358504286743‬  ·  jarno.satopaa@hus.fi

Always discuss trial participation with your own doctor first.

Locations (6)

Oulu University HospitalOulu, North Ostrobothnia, FinlandNot Yet Recruiting
Kuopio University HospitalKuopio, Northern Savonia, FinlandNot Yet Recruiting
Tampere University HospitalTampere, Pirkanmaa, FinlandNot Yet Recruiting
Turku University HospitalTurku, Southwest Finland, FinlandNot Yet Recruiting
Helsinki University HospitalHelsinki, Uusimaa, FinlandRecruiting
Karolinska University HospitalStockholm, Region Stockholm, SwedenNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06696079