Actively Recruiting
Evaluating the Benefit of Hypnoanalgesia Versus Neuroleptanalgesia During Hand Surgery
Led by GCS Ramsay Santé pour l'Enseignement et la Recherche · Updated on 2025-12-09
64
Participants Needed
1
Research Sites
167 weeks
Total Duration
On this page
Sponsors
G
GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead Sponsor
V
Vivactis M2Research
Collaborating Sponsor
AI-Summary
What this Trial Is About
This is a single-center, prospective, randomized, open-label study of two parallel groups of patients undergoing hand surgery: Group 1: locoregional anesthesia + neuroleptanalgesia Group 2: locoregional anesthesia + hypnoanalgesia Therapeutic benefit is based on VAS assessment of intraoperative anxiety.
CONDITIONS
Official Title
Evaluating the Benefit of Hypnoanalgesia Versus Neuroleptanalgesia During Hand Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 18 and 80
- Patient who has read and signed the consent form after a reflection period
- Patient undergoing outpatient hand surgery under locoregional anesthesia, such as upper limb trunk blocks (flexor teno synovectomy or endoscopic carpal tunnel surgery)
- Patient requiring sedation in addition to locoregional anesthesia
You will not qualify if you...
- Contraindication to locoregional anesthesia or to any sedative used in the study
- Pregnant or breastfeeding women, or women of childbearing age without effective contraception during the study
- Patients under court protection, guardianship, or curatorship
- Patients not affiliated with the French social security system
- Patients unable to understand information or provide written consent due to dementia, psychosis, disturbed consciousness, or language barriers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hôpital Privé Paul d'Egine
Champigny-sur-Marne, France, 94500
Actively Recruiting
Research Team
M
Mélanie FROMENTIN, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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