Actively Recruiting
Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults
Led by Centre Hospitalier Universitaire de Besancon · Updated on 2024-09-19
30
Participants Needed
1
Research Sites
185 weeks
Total Duration
On this page
AI-Summary
What this Trial Is 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.
CONDITIONS
Official Title
Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Programmed tonsillectomy surgery
You will not qualify if you...
- Congenital or acquired bleeding disorder
- Indication for uvulo-bike-pharyngo-plasty
- Contraindication to any study medication including pregnancy
- Allergy to analgesic treatments used in the study
- Ongoing analgesic treatment that cannot be interrupted
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU Besançon
Besançon, France, 25000
Actively Recruiting
Research Team
L
Laurent TAVERNIER, PU-PH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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