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Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults (DACAA)

C

Centre Hospitalier Universitaire de Besancon

Status

Enrolling

Conditions

Tonsillar Disorder

Treatments

Other: Assess pain management modalities in adult outpatient tonsillectomy surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT04853173
2020/542

Details and patient eligibility

About

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.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

ambulatory protocol after adult tonsillectomy
Experimental group
Description:
prescription of analgesics for outpatient procedure with hospital surveillance
Treatment:
Other: Assess pain management modalities in adult outpatient tonsillectomy surgery

Trial contacts and locations

1

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Central trial contact

Laurent TAVERNIER, PU-PH

Data sourced from clinicaltrials.gov

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