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Efficacy of Scalp Block on Hemodynamic Stability and Opioid Consumption During Craniotomy

U

University of Liege

Status

Unknown

Conditions

Craniotomy

Treatments

Procedure: Scalp block

Study type

Interventional

Funder types

Other

Identifiers

NCT02880566
anesneuro2016001

Details and patient eligibility

About

Prospective randomised double-blinded placebo-controlled trial on the efficacy of scalp blocks on hemodynamic stability and opioid consumption during and after craniotomy.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective craniotomy for supratentorial lesion

Exclusion criteria

  • Allergy to local anaesthetic
  • Psychiatric disease
  • Inability to consent
  • Uncontrolled intracranial hypertension

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

50 participants in 2 patient groups, including a placebo group

Treatment
Experimental group
Description:
Full scalp block performed with a total of 30 ml of levobupivacaine 0.33 %.
Treatment:
Procedure: Scalp block
Control
Placebo Comparator group
Description:
Full scalp block performed with a total of 30 ml of normal saline.
Treatment:
Procedure: Scalp block

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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