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OpenTrials
Completed

NCT Number: NCT05109416

Glossopharyngeal Nerve Block on Post Tonsillectomy Pain Among Egyptian Children

Tonsillectomy is one of most common performed surgical procedure in children . tonsillectomy or adenotonsillectomy have high incidence of Post operative pain , it is very important and significant problem because it can lead to decrease oral intake and dehydration

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Key information

Age range

7 year–15 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Faculty of Medcine

Minya, 61111, Egypt

About this study

Tonsillectomy is one of the most common performed surgical procedure in children. Tonsillectomy or adenotonsillectomy have high incidence of Post operative pain incidence . There is still debate about the optimal analgesia for this common procedure , different methods have been described including intraoperative anesthetic pain regimens , adjustment of surgical technique , intraoperative local anesthetic injection and use of pharmacotherapy post operative .

The main goal of the preventive analgesia is the pain releif with minimum side effect . The objective of this study is to investigate and compare the effect of Glossopharyngeal nerve block for relief of pain on children following adenotonsillectomy .

This is prospective , double blinded , randomized study

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • average weight is 10_50 kg
  • patient is generally stable
  • indication of tonsillectomy is recurrent tonsillitis
  • Ability to self report pain

Exclusion criteria

  • Hypersensitivity to bupivacaine
  • Obstructive sleep apnea syndrome
  • Pulmonary or cardic diseases

Treatment and study plan

Bupivacaine Hydrochloride 0.5% Injection Solution

Drug

Local anesthetic

Other names: Marcaine

saline 0.9%

Drug

Isotonic crystaloid

Other names: Saline 0.9 %

Primary outcomes

  1. The first call for analgesia

    Time frame: In 24 hours

    Pain assessment using VAS scale

Secondary outcomes

  1. The analgesic consumption

    Time frame: In 24 hours

    The total analgesic consumption for pain rest and swallowing

Sponsors and collaborators

Lead sponsor

Minia University

Other

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Nov 5, 2021
Registry last updated
Apr 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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