Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:13 PM
Ignite Modification Date:
2025-12-24 @ 1:13 PM
NCT ID:
NCT03053895
Eligibility Criteria:
Inclusion Criteria:
* Patients aged \>/= 18 years
* Presenting with symptomatic Chronic Subdural Hematoma confirmed on diagnostic imaging
* Able to provide informed consent or have a legal representatives available if unable to do so
Exclusion Criteria:
* Patients with acute or subacute subdural hematoma
* Patients with incidental or asymptomatic findings on CT; skull base, posterior fossa, or in the inter-hemispheric fissure Chronic Subdural Hematoma
* Patients with recurrent hematoma within 6 months of initial drainage
* Patients with Chronic Subdural Hematoma from previous intracranial surgery for different pathology Patients with subdural hygroma and non-hairline skull fracture over the Chronic Subdural Hematoma
* Patients with significant cognitive impairment or severe co-morbidity preventing improvement or follow-up
* Patients with hemorrhagic tendency that cannot be normalized
* Patients on anticoagulants, antithrombotics, or antiplatelets unless reversed or cleared - Patients who are unlikely to be available for a 6-month follow-up period
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03053895
Study Brief:
Protocol Section:
NCT03053895