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UNKNOWNNANCT04344132

Pre- vs. Postoperative Scalp Block for Pain Control After Supratentorial Craniotomy

Study was designed to evaluate optimal timing for selective scalp block in patients undergoing general anesthesia for supratentorial craniotomy.Pain score assessed by visual analog scale (VAS) preoper...

Lead sponsor: University of Roma La Sapienza•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

University of Roma La Sapienza

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Adult patients (\>18 years),
•presenting with supratentorial brain tumors scheduled for elective craniotomy under general anesthesia

Exclusion Criteria

•history of allergic reactions on local anesthetics;
•ASA status ≥ 3;
•depressed consciousness in pre- or postoperative period;
•aphasia (as investigators were not able to obtain VAS score).

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: April 15, 2020Terms

Trial snapshot

StatusUNKNOWN

PhaseNA

Enrollment50

Start dateApr 2020

Last updatedApr 15, 2020

Condition

Supratentorial Neoplasms

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 15, 2020Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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