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NCT06417723 Clinical Trial

Effect of Maxillary Nerve Block for Septoplasty

Post Operative Pain Clinical Trial

Official title:
Effect of Maxillary Nerve Block for Septoplasty

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06417723
Other study ID # ADYU-ANS-NY-04
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2024
Est. completion date September 15, 2024

Study information
Verified date May 2024
Source Adiyaman University Research Hospital
Contact Nezir Yilmaz
Phone 05068939496
Email yilmaznezirr@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study was to determine the effect of maxillary nerve blockage on both postoperative pain scores and recovery quality index in septoplasty operations. Thus, it was aimed to determine an alternative method that can be used in postoperative analgesia that will suppress postoperative pain complaints and increase the comfort level of patients after septoplasty operations.

Description:

Patients who were planned to be operated for septoplasty at Adıyaman University Training and Research Hospital, who were informed about the study and agreed to participate in the study with their written consent were included in the study. The patients who agreed to participate in the study were divided into two groups by closed envelope method and bilateral maxillary nerve blockade was planned to be performed using 10 cc 0.25% bupivacaine via suprazigomatic approach after providing airway safety in the block group with general anaesthesia applications in both groups. The haemodynamic values (blood pressure arterial, peak heart rate, peripheral oxygen saturation), postoperative numeric pain scores and postoperative quality of recovery index (QoR-15) values at the 24th hour were recorded and these values were compared in both groups. Thus, it was aimed to evaluate the effects of maxillary nerve blockade in septoplasty operations.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 60
Est. completion date September 15, 2024
Est. primary completion date August 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - ASA I-II , Septoplasty patints Exclusion Criteria: - ASA III-IV - Deny to participte in study

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Maxillary nerve block
It is aimed to reach the maxillary nerve trace with a peripheral nerve block needle using the suprazigomatic approach and to create a temporary block in the maxillary nerve with local anaesthetic injection.

Locations
Country Name City State
Turkey Adiyaman Training and Research Hospital Adiyaman

Sponsors (1)
Lead Sponsor Collaborator
Adiyaman University Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary The visual analog pain score postoperative pain scores will be assesed in 24 hours after surgery three months
Secondary Quality of recovery (QoR -15) a tool that asses recovery quality of paitent after surgery with 15 question will be used at 24th hour after surgery three months
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