Treatment of Chronic Pelvic Pain Due to Endometriosis by Transcutaneous Auricular Vagus Nerve Stimulation

ConditionEndometriosis
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age15+
SponsorHopital Foch

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Transcutaneous Auricular Vagus Nerve Stimulation

    Device

    Transcutaneous 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

72 Participants
are divided into 2 treatment groups
Group A: Transcutaneous auricular vagus nerve stimulationExperimental treatment 1 intervention
Group B: Standard treatmentNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

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"

Time frame
3 months after enrolment

Secondary outcomes

1

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"

Time frame
Day 1 and 3 months after enrolment
2

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"

Time frame
Day 1 and 3 months after enrolment
3

Efficacy on quality of life

Self assessement of quality of life using Endometriosis Health Profile-5

Time frame
Day 1 and 3 months after enrolment
4

Efficacy on quality of life

Self assessement of quality of life using EQ-5D scale

Time frame
Day 1 and 3 months after enrolment

Other outcomes

Sponsors and contacts

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