Clinical Trial

Echo-guided Scalp Blocks and Incidence of Postoperative Pain in Scheduled Supratentorial Intracranial Surgery.

Study acronym: ULTRASCALP
Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
Up to 30% of patients undergoing intracranial surgery present moderate to severe pain. In this type of surgery, the restriction of the pharmacopoeia, which goes against the concept of multimodal analgesia, results in the important use of opioids not without consequences in terms of complications. Numerous studies have highlighted the benefits of scalp blocks in postoperative pain. The originality of this study lies firstly in the fact that the scalp blocks will be guided by ultrasound and secondly, the incidence of severe pain after scalp blocks will be evaluated
Protocol Amendment History 2 changes
notable Primary completion pushed: 2027-10 -> 2028-07 2026-08-08
minor Completion pushed: 2028-01 -> 2028-09 2026-08-08
Trial Details
NCT Number NCT07149077
Lead Sponsor University Hospital, Bordeaux
Conditions Anesthesia , Analgesia
Enrollment 230 participants
Start Date 2026-09
Primary Completion 2028-07 (estimated)
Study Completion 2028-09 (estimated)
Updated on ClinicalTrials.gov 2026-08-07