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Clinical Trials in France / NCT07336303
Recruiting Not applicable

The Effect of Auriculotherapy on the Treatment of Postoperative Pain in Outpatient Rhizarthrosis Surgery

NCT07336303 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-02-01
Last updated
2026-07-24

Condition(s) studied

Thumb Arthritis

Investigational drug(s) / intervention(s)

outpatient prosthetic surgery for rhizarthrosis.real auricolotherysham auriculotherapy

outpatient prosthetic surgery for rhizarthrosis.: surgery / procedures : Outpatient surgery (thumb osteoarthritis). On the day of the procedure, the patient arrives on an outpatient basis, is positioned on a stretcher, and is then taken to the pre-anesthesia room where regional anesthesia is performed. The block is carried out under ultrasound guidance following a standardized protocol. The patient is then transferred to the operating room, where the tourniquet is applied. The surgical technique is endoscopic, following the AGEE method. At the end of the procedure, the surgeon places two or three absorbable sutures (4/0 or 5/0) on the thinnest areas of skin. The sutures are then covered with a dressing.

real auricolothery: 3 days before the intervention, patients will have an auriculotherapy session with an experimental group

sham auriculotherapy: 3 days before the intervention, patients will have an auriculotherapy session with an sham group

Study summary

Auriculotherapy has demonstrated promising potential in the management of postoperative pain. Additionally, one study reported encouraging outcomes regarding the reduction of anxiety levels among patients in primary healthcare settings. Nevertheless, further high-quality research is required to substantiate these findings and to support the integration of auriculotherapy into standardized therapeutic protocols.

The objective of this prospective, comparative, double-blind study is to assess the efficacy of auricular acupuncture in the management of postoperative pain following outpatient prosthetic surgery for rhizarthrosis

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Subject aged over 18 years * Patients hospitalized for endoscopic treatment of thumb carpometacarpal osteoarthritis (rhizarthrosis) * Patient with no prior history of auriculotherapy sessions * No participation in another clinical study * Subject affiliated with, or beneficiary of, a social security system * Agrees to complete all study questionnaires Exclusion Criteria: * Patient under 18 years of age * Unable to comply with medical follow-up required for the study * Adult subject under legal protection, guardianship, or trusteeship * Patient with neuropathic pain

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Benkessou Paris France Recruiting
Bizet Clinic Paris France Recruiting

More Clinique Bizet trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07336303 on ClinicalTrials.gov ↗ ← All trials in France