Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults

NCT ID: NCT04853173

Last Updated: 2024-09-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-09

Study Completion Date

2024-12-31

Brief Summary

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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

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Conditions

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Tonsillar Disorder

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Assess pain management modalities in adult outpatient tonsillectomy surgery
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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ambulatory protocol after adult tonsillectomy

prescription of analgesics for outpatient procedure with hospital surveillance

Group Type EXPERIMENTAL

Assess pain management modalities in adult outpatient tonsillectomy surgery

Intervention Type OTHER

use a post-operative analgesia protocol suitable for outpatient surgery. Namely a protocol of analgesia based on the taking of drugs per bone (by mouth) and not intravenous. Pain evaluation.

Interventions

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Assess pain management modalities in adult outpatient tonsillectomy surgery

use a post-operative analgesia protocol suitable for outpatient surgery. Namely a protocol of analgesia based on the taking of drugs per bone (by mouth) and not intravenous. Pain evaluation.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire de Besancon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU Besançon

Besançon, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Laurent TAVERNIER, PU-PH

Role: CONTACT

0381669360

Facility Contacts

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Laurent TAVERNIER

Role: primary

0381669360

Other Identifiers

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2020/542

Identifier Type: -

Identifier Source: org_study_id

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