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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT05126615
Other study ID # 2018-A01108-47
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date May 10, 2019
Est. completion date September 17, 2021

Study information

Verified date November 2021
Source Ramsay Générale de Santé
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Over the past decade, more and more healthcare professionals are using auriculotherapy as a preventative and effective therapy for pain. This therapy is applied by odontologists, anesthetists, surgeons, etc., to alleviate chronic pain. The effects of auriculotherapy are known in particular in reducing preoperative anxiety, pain in cancer patients and postoperative pain. The aim of this study is to assess the effectiveness of adding auriculotherapy to the standard global anesthetic protocol, compared to this single reference protocol, on the incidence at 3 months post-intervention of Chronic Post-Surgical Pain, in patients operated for a mastectomy with reconstruction immediate by latissimus dorsi flap.


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date September 17, 2021
Est. primary completion date August 6, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Women patient over 18 years-old - Patient scheduled for a mastectomy with immediate reconstruction by latissimus dorsi flap with or without symmetrization on the contralateral breast. - Patient affiliated or beneficiary of a social security scheme. - Patient who has given her free and informed consent. - Preoperative blood test showing no contraindication to the operation. Exclusion Criteria: - Refusal of the patient. - No indication for auriculotherapy: - Patient having a heavy treatment with neuroleptics, - Or tricyclic antidepressants which interfere with the action of auriculotherapy. - Patient undergoing long-term morphine treatment for chronic pain. - Patient with unweaned opioid addiction. - Chronic painful patient. - Protected patient: Major under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision; Hospitalized without consent. - Pregnant, breastfeeding or parturient woman. - Patient participating in another interventional study. - Patient who had already participated in this study as part of first breast surgery. - Patient receiving regular care by auriculotherapy

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Auriculotherapy
Application of a bolus of 5 µ of liquid nitrogen via a cryospray on the auriculotherapy points A4, C18, D9, C9, DIX, H13, G14 and FXVII, chosen according to a neurophysiological reasoning taking into account the surgical intervention performed and innervation of the anatomical region affected by the intervention.
Behavioral:
Chronic Post-Surgical Pain evaluation
Different questionnaires : BPI : Brief Pain Inventory DN4

Locations

Country Name City State
France Hôpital Privé Paul d'Egine Champigny-sur-Marne

Sponsors (1)

Lead Sponsor Collaborator
Ramsay Générale de Santé

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Presence, or not, of Chronic Post-Surgical Pain (DCPC) DCPC noted during the clinical examination of the 3rd postoperative month :
- score obtained at BPI : Brief Pain Inventory (9 items : many items with answers between 0 and 10)
3 months
Primary Presence, or not, of Chronic Post-Surgical Pain (DCPC) DCPC noted during the clinical examination of the 3rd postoperative month :
- score obtained at DN4 (neuropathic pain) : 4 different items
3 months
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