Viewing Study NCT04344132


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Study NCT ID: NCT04344132
Status: UNKNOWN
Last Update Posted: 2020-04-15
First Post: 2020-03-30
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Pre- vs. Postoperative Scalp Block for Pain Control After Supratentorial Craniotomy
Sponsor: University of Roma La Sapienza
Organization:

Study Overview

Official Title: Pre- vs. Postoperative Scalp Block for Pain Control After Supratentorial Craniotomy
Status: UNKNOWN
Status Verified Date: 2020-04
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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) preoperatively (baseline) and after extubation at 2, 6, 12 and 24 hours; time first request of a patient for rescue analgesia; intraoperative anesthetics and opioids consumption; awakening time; perioperative complications.
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: