Evaluation of the patient postoperative experience of two modes of WALANT-type anesthesia used in ambulatory upper-extremity surgery

Phase 1

• Conditions: MedDRA version: 20.0Level: PTClassification code 10013872Term: Dupuytren's contractureSystem Organ Class: 10028395 - Musculoskeletal and connective tissue disorders; MedDRA version: 20.0Level: PTClassification code 10007697Term: Carpal tunnel syndromeSystem Organ Class: 10029205 - Nervous system disorders; MedDRA version: 21.0Level: PTClassification code 10044654Term: Trigger fingerSystem Organ Class: 10028395 - Musculoskeletal and connective tissue disorders; MedDRA version: 20.0Level: PTClassification code 10058942Term: Ulnar tunnel syndromeSystem Organ Class: 10029205 - Nervous system disorders

• Registration Number: EUCTR2021-006493-23-FR
• Lead Sponsor: imes University Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-12-20
• Last Update Posted: 19 April 2022

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified