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Glossopharyngeal Nerve Block for Post -Tonsillectomy Pain Relief

NCT05435833 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2023-11-24

No results posted yet for this study

Summary

The aim of the present study is to evaluate the efficacy and safety of Ultra-sound guided submandibular parapharyngeal glossopharyngeal nerve block as regards time for first need of analgesic as a primary outcome as well as pain score, total postoperative analgesic requirement, and incidence of complications as secondary outcomes

Conditions

  • Analgesia

Interventions

PROCEDURE

bilateral ultrasound guided GPN block

a linear high frequency ultrasound probe will be initially positioned over the hyoid bone in the transverse plane, then the probe will be rotated to keep in line with the mandibular angle and the pharyngeal wall is identified by US. Using an in plane approach, a 22 G ,5 cm needle will be advanced till it reaches just superficial to the pharyngeal wall and 2.2 ml of 0.25% bupivacaine will be injected.

Sponsors & Collaborators

  • Gehan Morsy Eid

    collaborator UNKNOWN

  • Aliaa Muhammad Belal

    collaborator UNKNOWN

  • Mohamed Shebl Abdelghany

    collaborator UNKNOWN

  • Tanta University

    lead OTHER

Principal Investigators

  • Mona B El Mourad, MD · Tanta University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-11-05
Primary Completion
2023-08-01
Completion
2023-08-01

Countries

  • Egypt

Study Locations

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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 NCT05435833 on ClinicalTrials.gov