Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults

Not Applicable

• Conditions: Tonsillar Disorder

• Registration Number: NCT04853173
• Lead Sponsor: Centre Hospitalier Universitaire de Besancon

Brief Summary

No SFORL recommendation for adult ambulatory tonsillectomy. This study would allow the establishment of an ambulatory management during an adult tonsillectomy. This would allow a return home from J0 for the patient and therefore would improve the comfort of the patients and reduce the cost associated with a conventional hospitalization over several days.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-04-16
• Study First Submitted QC: 2021-04-20
• Study First Posted: 2021-04-21
• Study Start: 2021-05-28
• Status Verified: 2022-07
• Last Update Submitted: 2022-07-19
• Last Update Posted: 2022-07-20
• Primary Completion: 2022-11-28
• Study Completion: 2022-11-28

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• programmed Tonsillectomy surgery

Exclusion Criteria

• Congenital or acquired hemostasis disorder
• Indication of uvulo-bike-pharyngo-plasty
• Contraindication to the use of one of the protocol molecules including pregnancy
• Allergy to analgesic treatments used in the study
• Ongoing analgesic treatment that cannot be interrupted

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Assess pain management modalities in ambulatory tonsillectomy surgery in adults through post-operative pain assessment, with a defined analgesia and anesthesia protocol adapted to ambulatory management.	14 days	Pain measured by self-assessment by Analog Visual Scale (0-10). If score is under 4 = efficacity of ansthesia protocol

Trial Locations

Locations (1)

CHU Besançon; 🇫🇷 Besançon, France