MedTrace Logo

The Effect of Local Anesthesia on Postopanalgesia in Patients Using Head Holder

NCT07629713 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2026-06-05

No results posted yet for this study

Summary

Aim:The head holder used in neurosurgery operations causes pain in patients both peroperatively and postoperatively.Severe pain-related hemodynamic changes are seen in these participants.In our study, the investigators compared the effects of two different concentrations of lidocaine on the perioperative and postoperative hemodynamic response caused by the application of the head-holder, and the pain observed in the postoperative period.

Method: Ethics committee approval and participants consent were obtained. Lidocaine 0.5% in Group 1 and 1% lidocaine in Group 2 was administered subcutaneously, 3 ml to each three points, in a total of 9 ml. Postoperative analgesic efficacy and tramadol consumption amounts of different concentrations of lidocaine were compared in participants who used a head holder.

Conditions

  • Postoperative Pain, Acute

Interventions

DRUG

lidocaine was administered subcutaneously at 0.5% concentration.

In Group 1, lidocaine was administered subcutaneously at 0.5% concentration.

DRUG

lidocaine was administered subcutaneously at 1% concentration.

In Group 2, lidocaine was administered subcutaneously at 1% concentration.

Sponsors & Collaborators

  • Kocaeli University

    lead OTHER

Principal Investigators

  • DİLEK İÇLİ · PROFESSOR

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-10
Primary Completion
2019-01-15
Completion
2020-01-16

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07629713 on ClinicalTrials.gov