Rates of Repeated Operation for Isolated Subdural Hematoma Among Older Adults.
Jared Knopman, Thomas W Link, Babak B Navi...
https://pubmed.ncbi.nlm.nih.gov/30646255/Actively Recruiting
Led by Sohag University · Updated on 2025-08-27
80
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are comparing two anesthesia methodsscalp block and general anesthesiain adults aged 18 to 75 years undergoing burr-hole evacuation for subdural hematoma. This study aims to determine which approach may be preferable during this surgical procedure. It is a prospective randomized trial sponsored by Sohag University, focusing on anesthesia techniques for this condition. One group will receive general anesthesia induced with intravenous propofol and fentanyl, followed by cisatracurium and endotracheal intubation. The other group will receive a scalp block targeting six pairs of sensory nerves supplying the scalp using local anesthetics lidocaine and bupivacaine at specific anatomical landmarks. The study compares these two anesthesia methods during the operation. Participants will be monitored for outcomes 24 hours after surgery. Evaluations will include clinical assessments related to anesthesia effectiveness and safety. The trial follows patients during the immediate postoperative period to compare the impact of the two anesthesia techniques on their recovery and condition after subdural hematoma evacuation.
CONDITIONS
Scalp Block Versus General Anesthesia in Patients Undergoing Evacuation of Subdural Hematoma Via Burr Hole
M
Mohamed H elsayed, Resident
A
Abdel Rahman H Abdel Rahman, Professor
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Sohag University
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo either general anesthesia or scalp block during the evacuation of subdural hematoma via burr hole.
1 surgical visit (in-person)
Duration - 24 hours after operation
Participants are monitored for 24 hours after the operation for outcomes related to the anesthesia method used.
Approximately 1 post-operative visit
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/33066943/Sohag University
Lead Sponsor