About this trial
6-10% of women of childbearing age suffer from endometriosis, which is mainly manifested by dysmenorrhea, non-menstrual pelvic pain and dyspareunia. Several treatment strategies, including surgical ones, are proposed but they are sometimes insufficient because endometriosis-related pain is frequently accompanied by sensitization. Endometriosis surgery, when indicated, is therefore changeably effective, even though the lesions have been completely resected. Patients therefore consult Pain Units seeking for the effective treatment as the pain persist even after surgical management of endometriosis.
Vagus nerve stimulation is a non-invasive technique that includes an anti-inflammatory effect and a modulation of neurotransmitter production (adrenaline, norepinephrine; serotonin, acetylcholine). Yuan and Silberstein published a general review on the technique. Migraine and depression are one of the selected indications. In addition, Napadow et al. published favourable results in a short series of patients with chronic pelvic pain. The Investigators of this study have treated some patients with this technique with a result deemed satisfactory which leads to propose a randomized study to confirm this impression.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Women aged >= 15 years
With chronic pelvic pain and/ or dysmenorrhoea and/ or dyspareunia
Who has been cared for by a gynecologist in one of the institutions participating in the study
Diagnosed with endometriosis
Disqualifiers
contraindication to the use of transcutaneous auricular vagus nerve stimulation (cardiac pathology, asthmatic patient)
pregnant or breastfeeding women
patient undergoing in vitro fertilization
associated pathology requiring long-term analgesic treatment
Trial design
Parallel
Treatments tested in this trial
Transcutaneous Auricular Vagus Nerve Stimulation
DeviceTranscutaneous Auricular Vagus Nerve Stimulation has an eartip connected to an external stimulator. The device used in this study is the TENS Eco Plus commercialized by Schwa Medico and European Compliance (CE) marked. The electrode is positioned in the cymba concha of the left ear.
Treatment groups
Trial outcomes
Primary outcomes
Change of symptoms related to the pelvic pain
Self assessement of change using Patient's Global Impression of Change (PGIC) scale in which patients rate the improvement of their symptoms related to their pelvic pain from "No change or it get worse" to "A great deal better, and a considerable improvement that has made all the difference" . A favorable result will be "Better, and a definite improvement that has made a real and worthwhile difference" or "A great deal better, and a considerable improvement that has made all the difference"
Secondary outcomes
Efficacy on pain
Self assessement of pain using Endometriosis-associated pelvic pain scale on which patients rate their current pain intensity from 0 "No pain" to 10 "worst possible pain"
Efficacy on severity of patient's symptoms
Physician assessement of severity of patient's symptoms using Global Clinical Impressions-Severity scale on which physicians rate the severity of patient's symptoms from "not evaluated" to "Among the sickest patients"
Efficacy on quality of life
Self assessement of quality of life using Endometriosis Health Profile-5
Efficacy on quality of life
Self assessement of quality of life using EQ-5D scale
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