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Comparison of Effects of Scalp Block and Intravenous Esmolol on Hemodynamic Response Following the Skull Pins Application for Elective Supratentorial Craniotomy

K

Khon Kaen University

Status

Completed

Conditions

Hemodynamic Instability

Treatments

Procedure: Scalp block
Drug: Esmolol

Study type

Interventional

Funder types

Other

Identifiers

NCT06268275
HE651314

Details and patient eligibility

About

The goal of this clinical trial is to compare hemodynamic response (MAP, SBP, DBP and HR) between scalp block and intravenous esmolol while skull pins application in patients undergoing elective supratentorial craniotomy under general anesthesia.

Enrollment

90 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18-65 years old
  • BMI 18-30 kg/m2
  • American Society of Anesthesiologists (ASA) status I-III
  • Elective supratentorial craniotomy under general anesthesia
  • Required application of skull pins

Exclusion criteria

  • Poor controlled hypertensive condition (Baseline BP ≥ 160/110 mmHg)
  • Thrombocytopenia / Coagulopathy
  • Preoperative atrioventricular block (More than 2nd degree AV block)
  • Emergency surgery
  • Posterior fossa / Intracranial aneurysm surgery
  • Pregnancy
  • Chronic use of pain control
  • Contraindication to beta-blockers
  • Allergy to the drugs used in the study

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

90 participants in 2 patient groups

Group S
Experimental group
Description:
Receive 30 ml of 0.25% bupivacaine with 1% lidocaine (1:1) with adrenaline 1:200,000 infiltration for 10 minutes before skull pins application.
Treatment:
Procedure: Scalp block
Group E
Active Comparator group
Description:
Receive intravenous esmolol 1 mg/kg bolus over 1 minute before skull pins application.
Treatment:
Drug: Esmolol

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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