CompletedNot Applicable

Glossopharyngeal Nerve Block for Post -Tonsillectomy Pain Relief

Egypt50 participantsStarted 2022-11-05

Plain-language 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

Who can participate

Age range21 Years – 65 Years

SexALL

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Inclusion Criteria: * Patients classified by the American society of Anesthesiologists ASA I and II patients * Scheduled for tonsillectomy procedure Exclusion Criteria: * Patients' refusal * History of diabetes mellitus, * Cardiac, liver or renal impairment * Obstructive sleep apnea syndrome * Swallowing difficulty * Intake of chronic pain medications or substance abuse * Bleeding disorders * Hypersensitivity to the used medication

What they're measuring

Onset of 1st analgesic request

Timeframe: up to 24 hours postoperative

Trial details

NCT IDNCT05435833

SponsorTanta University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-08-01

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