Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de Besancon

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

programmed Tonsillectomy surgery

Disqualifiers

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

Trial design

Design model

Single group

Treatments tested in this trial

  • Assess pain management modalities in adult outpatient tonsillectomy surgery

    Other intervention

    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.

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: ambulatory protocol after adult tonsillectomyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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.

Pain measured by self-assessment by Analog Visual Scale (0-10). If score is under 4 = efficacity of ansthesia protocol

Time frame
14 days

Secondary outcomes

Other outcomes

Sponsors and contacts

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