Clinical Trial

When to Block? Timing of Scalp Block in Craniotomy

Completed
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Summary
This study aims to evaluate the effect of scalp block timing-Group 1 will receive a pre-pinning scalp block, while Group 2 will receive a pre-emergence scalp block.-on postoperative recovery quality in patients undergoing supratentorial tumor craniotomy. The recovery quality will be assessed using the validated Quality of Recovery-40 (QoR-40) questionnaire. A total of 60 patients, aged 18-80 years, classified as ASA I-III and with a Glasgow Coma Scale (GCS) score of 15 upon admission to the recovery unit, will be enrolled. The primary outcome is the QoR-40 score. Secondary outcomes include hemodynamic changes and pain intensity measured by the Visual Analog Scale (VAS).
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-06-27.
Status change: Not Yet Recruiting → Completed 2026-07-07
Trial Details
NCT Number NCT07043621
Lead Sponsor Sakarya University
Conditions Scalp Block, Regional Anesthesia, Craniotomy Surgery, QoR-40
Enrollment 60 participants
Start Date 2025-07-01
Primary Completion 2026-02-25 (estimated)
Study Completion 2026-02-27 (estimated)
Updated on ClinicalTrials.gov 2026-07-09