Safety and Efficacy of Aspirin Continuation or Discontinuation in Conservative Treatment for Chronic Subdural Hematoma: A Randomized Clinical Trial

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This clinical study aims to learn about the efficacy and safety of aspirin continuation or discontinuation in conservative treatment for chronic subdural hematoma. All participants received standard conservative treatment for chronic subdural hematoma, with a randomized intervention to either continue or discontinue aspirin administration. By participating in this study, participants can receive additional scientific guidance on aspirin medication management beyond routine conservative treatment, thereby optimizing individualized therapy.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥18 years, male or female;

• Confirmed diagnosis of chronic subdural hematoma (cSDH) by cranial CT and/or MRI;

• Intended for conservative management (i.e., no surgical evacuation indication at enrollment);

• Regular aspirin use at enrollment;

• Informed consent signed by the patient or legal representative.

Locations
Other Locations
China
Xuanwu Hospital Capital Medical University
RECRUITING
Beijing
Tianjin Medical University General Hospital
RECRUITING
Tianjin
Contact Information
Primary
Tao Liu, MD
TLiu1@georgeinstitute.org.au
+86-18302204804
Time Frame
Start Date: 2025-10-15
Estimated Completion Date: 2028-12
Participants
Target number of participants: 143
Treatments
Experimental: Aspirin Continuation Group
All participants received standard conservative treatment for chronic subdural hematoma, with a randomized intervention to continue aspirin administration. This group of participants received oral administration of aspirin at a dose of 100 mg per day.
Experimental: Aspirin Discontinuation Group
All participants received standard conservative treatment for chronic subdural hematoma, with a randomized intervention to discontinue aspirin administration. This group of participants did not use aspirin during the treatment period.
Sponsors
Leads: Tao Liu
Collaborators: Xuanwu Hospital, Beijing, Tianjin Medical University General Hospital

This content was sourced from clinicaltrials.gov