Evaluation of the Analgesic Effect of Direct Current Stimulation in the Treatment of Pelvic Pain, Comparing Three Groups: Trans-spinal Stimulation, Ganglionic Stimulation, and Placebo. A Randomized Double-blind Study
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Non-invasive device-based neuromodulation.
- Кому может быть актуально
- Состояния в реестре: Chronic Pelvic Pain. Базовые параметры: 18 лет — 85 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Франция
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Обзор
The purpose of this study is to evaluate the analgesic effectiveness of direct current stimulation (tsDCS) in the treatment of pelvic pain by comparing three groups: * Trans-spinal tsDCS stimulation, * Ganglionic tsDCS stimulation, * Placebo (sham) tsDCS stimulation.
Подробное описание
Conduct of study:
Entry into the study: After informed consent, patients will be randomised. The physician responsible for conducting neurostimulation sessions will make the randomization via Redcap. Only this physician will have the knowledge of the group allocated to the patient.
Baseline : Patients, will record on a diary form, a daily Visual Numeric Scale(VNS) of Pain Intensity for 1 week.
Treatment sessions: after the baseline, sessions of neurostimulation will begin for 5 weeks.
After the end of neurostimulation sessions, patients will be followed for 2 weeks.
Throughout their participation in the study, patients will plot on a diary form their daily VNS.
Вмешательства
- Устройство Non-invasive device-based neuromodulation
Direct current stimulation (tsDCS) protocol consist of one daily session for five consecutive days during the first week, followed by one session per week until week 5, after which the treatment period ends and post-treatment follow-up begins.
Первичные конечные точки
- Evolution of Pain [Срок оценки: Pain progression will be assessed from week 1 (before treatment) to week 7 (end of treatment)]
Вторичные конечные точки (9)
- Rate of Responding Patients [Срок оценки: week 7 compared with baseline]
- Evaluation of the analgesic effect maintenance [Срок оценки: Between Week 5 (end of treatment) and Weeks 6 to 7 (post-treatment follow-up).]
- Assessment of Overall Patient Improvement. [Срок оценки: Day 50 from the beginning of tsDCS treatment compared to baseline]
- Quality of Life Improvement. [Срок оценки: Day 50 from the beginning of tsDCS stimulation treatment compared to baseline]
- Evolution of Anxiety and Depressive Traits. [Срок оценки: Day 50 from the beginning of tsDCS treatment compared to baseline]
- Evolution of Symptomatological Profiles of Neuropathic Pain. [Срок оценки: Day 50 from the beginning of tsDCS treatment compared to baseline]
- Sympathetic Autonomic System Injury and Small Fiber Neuropathy. [Срок оценки: Day 50 from the beginning of tsDCS treatment compared to baseline.]
- Autonomous System Assessement. [Срок оценки: Day 50 from the beginning of tsDCS treatment compared to baseline.]
- Evolution of the use of analgesic treatments. [Срок оценки: From baseline to day 50.]
Критерии участия
Критерии включения
- Patient aged 18 to 85 years, suffering from pelvic pain for more than one year (excluding musculoskeletal causes).
- Patient with stable ongoing medication (analgesic or otherwise) for at least one month.
- Patient for whom lack of response to conventional treatments has led the pain specialist or referring physician to consider non-pharmacological therapeutic options.
- Patient reporting a pain intensity score >3 on the Numeric Visual Pain Scale (NVPS) during pre-screening.
- Patient affiliated with the national health insurance system or an equivalent scheme.
- Patient who has provided written informed consent.
Критерии исключения
- History of drug addiction.
- History of psychiatric disorders likely to interfere with the proper conduct of the study.
- Patient with skin lesions in the lumbar region.
- Person unable to understand the study protocol.
- Individuals covered by Articles L1121-5 to L1121-8 of the French Public Health Code, corresponding to all protected persons: pregnant women, women in labor, breastfeeding mothers, individuals deprived of liberty by judicial or administrative decision, or under legal protection.
- Subject currently in the exclusion period of another clinical trial
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Тройное слепое
- Основная цель
- Поддерживающая терапия
Центры проведения
Франция · 2 центра
- Clinical Neurophysiology Unit, Henri Mondor University Hospital, Assistance Publique-Hôpit — Créteil
- Pain Management Center, Grenoble Alpes University Hospital (CHU Grenoble Alpes) — Grenoble
Публикации
- Hodaj H, Payen JF, Lefaucheur JP. A Case of Long-Term Treatment of Chronic Pain Syndrome by Anodal tDCS of the Motor Cortex, Previously Resistant to High-Frequency rTMS and Implanted Spinal Cord Stimulation. Brain Stimul. 2016 Jul-Aug;9(4):618-20. doi: 10.1016/j.brs.2016.02.008. Epub 2016 Mar 22. No abstract available. PMID 27101725
- Lefaucheur JP, Antal A, Ayache SS, Benninger DH, Brunelin J, Cogiamanian F, Cotelli M, De Ridder D, Ferrucci R, Langguth B, Marangolo P, Mylius V, Nitsche MA, Padberg F, Palm U, Poulet E, Priori A, Rossi S, Schecklmann M, Vanneste S, Ziemann U, Garcia-Larrea L, Paulus W. Evidence-based guidelines on the therapeutic use of transcranial direct current stimulation (tDCS). Clin Neurophysiol. 2017 Jan; PMID 27866120
- Hodaj H, Payen JF, Mick G, Vercueil L, Hodaj E, Dumolard A, Noelle B, Delon-Martin C, Lefaucheur JP. Long-term prophylactic efficacy of transcranial direct current stimulation in chronic migraine. A randomised, patient-assessor blinded, sham-controlled trial. Brain Stimul. 2022 Mar-Apr;15(2):441-453. doi: 10.1016/j.brs.2022.02.012. Epub 2022 Feb 25. PMID 35219923
- Hodaj H, Payen JF, Hodaj E, Dumolard A, Maindet C, Cracowski JL, Delon-Martin C, Lefaucheur JP. Long-term treatment of chronic orofacial, pudendal, and central neuropathic limb pain with repetitive transcranial magnetic stimulation of the motor cortex. Clin Neurophysiol. 2020 Jul;131(7):1423-1432. doi: 10.1016/j.clinph.2020.03.022. Epub 2020 Apr 10. PMID 32387962
- Hodaj H, Payen JF, Dumolard A, Delon-Martin C, Lefaucheur JP. Treatment of pudendal neuralgia by high-frequency rTMS of the medial wall of motor cortex bilaterally using an angled figure-of-eight coil. Brain Stimul. 2020 Sep-Oct;13(5):1412-1413. doi: 10.1016/j.brs.2020.07.009. Epub 2020 Jul 23. No abstract available. PMID 32712341
- Hodaj H, Payen JF, Hodaj E, Sorel M, Dumolard A, Vercueil L, Delon-Martin C, Lefaucheur JP. Long-term analgesic effect of trans-spinal direct current stimulation compared to non-invasive motor cortex stimulation in complex regional pain syndrome. Brain Commun. 2023 Jul 1;5(4):fcad191. doi: 10.1093/braincomms/fcad191. eCollection 2023. PMID 37545548
- Guidetti M, Ferrucci R, Vergari M, Aglieco G, Naci A, Versace S, Pacheco-Barrios K, Giannoni-Luza S, Barbieri S, Priori A, Bocci T. Effects of Transcutaneous Spinal Direct Current Stimulation (tsDCS) in Patients With Chronic Pain: A Clinical and Neurophysiological Study. Front Neurol. 2021 Sep 6;12:695910. doi: 10.3389/fneur.2021.695910. eCollection 2021. PMID 34552550
- Rahman MA, Tharu NS, Gustin SM, Zheng YP, Alam M. Trans-Spinal Electrical Stimulation Therapy for Functional Rehabilitation after Spinal Cord Injury: Review. J Clin Med. 2022 Mar 11;11(6):1550. doi: 10.3390/jcm11061550. PMID 35329875
Идентификаторы
NCT: NCT07237165 · 38RC24.0366