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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-04-20

Study Completion Date

2020-12-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Supratentorial Neoplasms

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Interventions

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Scalp Block

standard practice of controll the pain after surgery. Block of the nerve emergences.

Intervention Type PROCEDURE

Eligibility Criteria

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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).

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No