CHU Besançon
Besançon, 25000, France
Location status: Recruiting
NCT Number: NCT04853173
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Besançon, 25000, France
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: 14 days
Pain measured by self-assessment by Analog Visual Scale (0-10). If score is under 4 = efficacity of ansthesia protocol
Contact information is provided by the study sponsor or research team.
Centre Hospitalier Universitaire de Besancon
Other
Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults: External Pilot Study
Acronym: DACAA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07574476
Tonsillar Disorder
Columbus, Ohio, United States
View Trial Details