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Recruiting Not applicable

Scalp Block Versus General Anesthesia in Patients Undergoing Evacuation of Subdural Hematoma Via Burr Hole

NCT07143799 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-08-11
Last updated
2025-08-27

Condition(s) studied

Subdural Hematoma

Investigational drug(s) / intervention(s)

Cisatracurium →scalp block

Cisatracurium: Induction of general anesthesia will be done by IV propofol 2-2.5 mg / kg and IV fentanyl lug/kg. After IV Cis-atracurium 0.15mg/kg, endotracheal intubation will be done.

scalp block: The scalp block will target six pairs of sensory nerves that innervate the scalp: the supraorbital nerve, supratrochlear nerve, auriculotemporal nerve, zygomaticotemporal nerve, greater occipital nerve, and lesser occipital nerve. Local anesthetic (2% lidocaine and bupivacaine) will be infiltrated at specific anatomical landmarks corresponding to the course of each nerve.

Study summary

this study amis to compare between Scalp block versus general anesthesia in patients undergoing evacuation of subdural hematoma via burr hole.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria * Age from 18 to 75 years old. * Both sexes. * American Society of Anesthesiologists (ASA) physical status II-III. * Patients with subdural hematoma undergoing burr-hole evacuation Exclusion Criteria: * Patients with a history of known sensitivity to study drugs. * Glasgow Coma Scale (GCS) \<8 * Impaired coagulation profile. * Any degree of heart block. * Infection at site of injection

Primary outcome measure(s)

  • The aim of this prospective randomized study is to compare Scalp block versus general anesthesia in patients undergoing evacuation of subdural hematoma via burr hole. — 24 hours after operation
    Post operative scale by The Glasgow Coma Scale (GCS) and post operative hemodynamics.

Trial sites (1)

FacilityCityRegionStatus
Sohag university hospital Sohag Egypt Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07143799 on ClinicalTrials.gov ↗ ← All trials in Egypt