RecruitingNot ApplicableNCT06127628

Effectiveness of Ultrasound-guided Scalp Block for Supratentorial Craniotomy

Effectiveness of Ultrasound-guided Scalp Block for Supratentorial Craniotomy: a Randomised Controlled Trial


Sponsor

University Malaysia Sarawak

Enrollment

60 participants

Start Date

Apr 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Pain management in patients undergoing neurosurgery is a very important issue. The effectiveness of USG-guided scalp blocks for pain management in craniotomy surgery is currently not known. The purpose of this clinical trial is to evaluate the effectiveness of ultrasound-guided scalp block when performed in patients who undergo supratentorial craniotomies.


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • All American Society of Anesthesia class I to III patients undergoing elective supratentorial craniotomies under general anaesthesia.

Exclusion Criteria10

  • Refusal to participate in the study
  • Contraindications to the performance of scalp block, such as local infections
  • Allergy to ropivacaine hydrochloride
  • Age < 18 years old
  • Undergoing emergency craniotomies, posterior fossa surgery, or burr holes surgery
  • Pre-existing chronic pain (defined as persistent or recurrent pain lasting > 3 months)
  • History of drug addiction (illicit substances and opioids use) or chronic alcohol abuse
  • Presence of uncontrolled systemic arterial hypertension, severe cardiovascular disease, severe kidney or severe liver diseases
  • Predicted to require postoperative ventilation in the intensive care unit
  • Psychiatric disorders, serious neurological diseases, or reduced consciousness GCS < 14

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Interventions

PROCEDUREUltrasound-guided scalp block with ropivacaine 0.375%

Scalp block will be performed under USG guidance, using the technique described by Tsan et al. The block needle used will be an echogenic block needle, with a length of 50 mm, and a diameter of 22 G. Trained personnel comprising of the investigators in this study will perform the scalp block. Using ultrasound to identify landmarks, ropivacaine 0.375% will be administered in volumes of 1.5 ml to 3 ml. The nerves targeted will be the supraorbital, supratrochlear, zygomaticotemporal, auriculotemporal, greater auricular, lesser occipital, greater occipital and third occipital nerves.


Locations(1)

Sarawak General Hospital

Kuching, Sarawak, Malaysia

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NCT06127628


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