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Chronic Subdural Hematoma clinical trials

View clinical trials related to Chronic Subdural Hematoma.

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NCT ID: NCT04966546 Active, not recruiting - Clinical trials for Chronic Subdural Hematoma

Targeting Spreading Depolarization After Chronic Subdural Hematoma Surgery (TASD)

TASD
Start date: June 1, 2022
Phase: Early Phase 1
Study type: Interventional

Chronic Subdural Hematoma (cSDH) is an extremely common problem, particularly in the aging population, where fluid like collections compress the brain, frequently requiring surgical drainage. After drainage, 25-50% of patients experience post operative neurologic deficits such as weakness or confusion that are often not explained by problems such as seizure, stroke, or mass effect from the fluid and blood. Recent subdural recordings have demonstrated that some of these neurological deficits may be related to waves of spreading depolarization (SD), which cause temporary neurological dysfunction. Our overall objective is to examine the relationship between neurological deficits and SD and to assess feasibility of a pilot trial to determine if a strategy of NMDA-R antagonism can effectively reduce SD and improve clinical recovery.

NCT ID: NCT04816591 Active, not recruiting - Clinical trials for Chronic Subdural Hematoma

Middle Meningeal Artery Embolization for the Treatment of Subdural Hematomas With TRUFILL® n-BCA

MEMBRANE
Start date: May 27, 2021
Phase: N/A
Study type: Interventional

This is a prospective, multi-center, open-label, randomized controlled study in which subjects can receive standard of care (SOC) alone or SOC and TRUFILL n-BCA MMA embolization for the treatment of chronic subdural hematomas (cSDH).

NCT ID: NCT03788005 Active, not recruiting - Clinical trials for Chronic Subdural Hematoma

GET-UP Trial: Impact of an Early Out-of-bed Paradigm in Postoperative Outcomes of Chronic Subdural Hematomas

GET-UP
Start date: April 7, 2019
Phase: N/A
Study type: Interventional

Compare rates of medical complications, recurrence and outcome in 2 randomized groups of patients with surgical chronic subdural hematomas. The intervention group will be assigned to early mobilization (within 12 hours of the surgical procedure). The control group will be assigned to bed rest for 48 hours.