About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
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
Trial design
Parallel
Treatments tested in this trial
outpatient prosthetic surgery for rhizarthrosis.
Procedure/Surgerysurgery / 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
Other intervention3 days before the intervention, patients will have an auriculotherapy session with an experimental group
sham auriculotherapy
Other intervention3 days before the intervention, patients will have an auriculotherapy session with an sham group
Treatment groups
Trial outcomes
Primary outcomes
Assessment of pain reduction using the Numerical Rating Scale (NRS) questionnaire during the postoperative period from Day 1 to Day 3. From Day 1 to Day 3, Based on Real or Sham Auriculotherapy Sessions
The Numerical Rating Scale (NRS) is a validated, unidimensional tool used to assess pain intensity. Patients are asked to rate their pain by selecting a number that best reflects its severity. Valeur minimale : 0 - corresponds to "no pain". Valeur maximale : 10 - corresponds to "the worst pain imaginable". Interprétation générale : 0 : No pain 1-3 : Mild pain 4-6 : Moderate pain 7-10 : Severe pain
Secondary outcomes
Assessment of the onset of neuropathic pain using the DN4 questionnaire during follow-up.
The DN4 questionnaire is a validated diagnostic instrument designed to differentiate neuropathic pain from nociceptive pain. It comprises 10 items, including 7 symptom-based descriptors (e.g., burning, painful cold, electric shocks, tingling, pins and needles, numbness, itching) and 3 clinical examination findings (hypoesthesia to touch, hypoesthesia to pinprick, and pain provoked by brushing). Minimum score: 0, indicating the absence of neuropathic pain features. Maximum score: 10, indicating the presence of all evaluated neuropathic characteristics. Interpretation: A score ≥ 4 is considered the diagnostic threshold and is associated with a high probability of neuropathic pain, based on the tool's validated sensitivity and specificity. Scores \< 4 suggest that neuropathic pain is unlikely.
Assessment of analgesic consumption (number, name, and analgesic step) from the end of the hand regional anesthesia until Day 3, and again at one month
analgesic consumption (number, name, and analgesic step)
Assessment of patient satisfaction using the CGI-C scale.
The CGI-C is a validated clinician-rated scale used to assess the patient's overall change in clinical status compared with baseline. It provides a global, integrative judgment that incorporates all available clinical information, including symptoms, functioning, and therapeutic response. Minimum score: 1 - Very much improved Maximum score: 7 - Very much worse Interpretation: 1-2: Marked or clear improvement 3: Minimal improvement 4: No change 5: Minimal worsening 6-7: Clear to marked worsening
Assessment of postoperative anxiety reduction between the two groups using the State-Trait Anxiety Inventory (STAI) score.
State-Trait Anxiety Inventory (STAI - Form Y) The State-Trait Anxiety Inventory is a validated psychometric instrument designed to assess two distinct components of anxiety: State Anxiety (STAI-S): reflects a transient emotional condition characterized by feelings of tension, apprehension, and heightened autonomic activity. It measures anxiety "right now, at this moment." Trait Anxiety (STAI-T): reflects a stable predisposition to perceive situations as threatening and to respond with elevated anxiety across time. Each subscale contains 20 items, rated on a 4-point Likert scale. * Minimum score: 20 * Maximum score: 80 Interpretation: Higher scores indicate higher levels of anxiety. * 20-37: low anxiety * 38-44: moderate anxiety * ≥ 45: high anxiety
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