Adjuvant Treatment of Postoperative Pain Following Endoscopic Carpal Tunnel Surgery by Auriculotherapy

NCT06693167 | Completed

• 1 other identifier: 0990-0279
• Study Type: observational
• Target: 38
• Locations: 0 countries
• Sites: N/A

Brief Summary

Retrospective study on the effect of auriculotherapy on postoperative pain after carpal tunnel surgery

Conditions

Chirurgical Intervention; Auriculotherapy

Outcome Measures

Primary Outcomes (1)

• demonstrate the effectiveness of auriculotherapy in the management of postoperative pain

  pain assessment scale

  Day1, Day2 and Day 3

Secondary Outcomes (1)

• reducing the consumption of painkillers

  Day1, Day2 and Day 3

Interventions

chirurgie canal carpien PROCEDURE

study compares a group of patients who received a preoperative auriculotherapy session followed by standard analgesic treatment to a group who received only standard analgesic treatment, and this, during the three days following surgery (D1, D2, and D3).

Eligibility Criteria

• Age: 18 Years - 84 Years
• Sex: all
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients suffering from carpal tunnel syndrome for whom elective endoscopic surgery is indicated

You may qualify if:

• Patients aged 18 to 84 years.
• Patients suffering from carpal tunnel syndrome for whom elective endoscopic surgery is indicated

You may not qualify if:

• Have already benefited from an auriculotherapy session.
• Presence of cryoglobulinemia.
• Presence of Raynaud's syndrome.
• Presence of hemoglobinopathy (hemoglobin and capillary abnormalities).
• Allergy to cold.
• Presence of dermatological lesions on the auricle of one of the two ears

Sponsors & Collaborators

• Clinique Bizet: lead

Related Links

• 6- Sator-Katzenschlager, S. M., Scharbert, G., Kozek-Langenecker, S. A., Dolezal, S., Michalek-Sauberer, A., Kress, H. G., \& Heinze, G. (2003). The short- and long-term benefit in chronic low back pain through adjuvant electrical versus manual auricular

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: OTHER
• Target Duration: 7 Days
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 12, 2024
• First Posted: November 18, 2024
• Study Start: October 1, 2016
• Primary Completion: May 1, 2017
• Study Completion: June 1, 2017
• Last Updated: November 18, 2024

Record last verified: 2024-10