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Набор скоро начнётся NCT07074561

The Synergism and Attenuation Effects of Electroacupuncture in the Treatment of Trigeminal Neuralgia

Без фазы С лечением Trigeminal Neuralgia

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: CBZ placebo, CBZ, Electroacupuncture, Sham electroacupuncture.
Кому может быть актуально
Состояния в реестре: Trigeminal Neuralgia. Базовые параметры: 18 лет — 75 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
Список центров уточняется — проверьте первичный протокол.
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

The Synergism and Attenuation Effects of Electroacupuncture in the Treatment of Trigeminal Neuralgia:Protocol for a Multicentre Pilot Randomised Controlled Trial

Обзор

Trigeminal neuralgia (TN), characterized by its refractory nature and recurrence, frequently leads to anxiety, depression, and insomnia, thereby significantly diminishing patients' quality of life and potentially inducing self-harm. Carbamazepine (CBZ) is the first-line medication for TN, yet it presents adverse effects such as addiction and the absence of analgesic effects upon cessation. Acupuncture, particularly electroacupuncture(EA), has demonstrated efficacy in TN treatment, although its therapeutic outcomes are influenced by various factors. This multicenter, randomized controlled trial aims to evaluate the synergistic efficacy-enhancing and toxicity-reducing effects of the optimized protocol when combined with carbamazepine (CBZ) in treating trigeminal neuralgia (TN), thereby proposing novel therapeutic refinements for electroacupuncture treatment regimens in TN management.

Вмешательства

  • Препарат CBZ placebo
    Patients received oral administration of one 100 mg placebo tablet three times daily (TID) after meals for four consecutive weeks.
  • Препарат CBZ
    In the EA + CBZ + placebo group, patients received oral carbamazepine (CBZ) at a dosage of 100 mg per tablet three times daily (TID) after meals for 4 consecutive weeks. In the sham EA + CBZ group, patients were administered oral CBZ at 200 mg per dose TID after meals for the same 4-week duration.
  • Процедура Electroacupuncture
    The primary acupoints selected were the affected side's Sibai (ST2), Xiaguan (ST7), and Dicang (ST4). Based on the affected nerve branch, additional acupoints were chosen: for the ophthalmic branch, Tongziliao (GB1); for the maxillary branch, Quanliao (SI18); and for the mandibular branch, Jiache (ST6). Distal acupoints included bilateral Hegu (LI4) and Waiguan (SJ5). Electroacupuncture was applied based on the affected nerve branch. For the ophthalmic branch, the local acupoints selected were X
  • Процедура Sham electroacupuncture
    In this group, superficial needling (0.5-1 mm depth) was performed at non-meridian points located 1 cm lateral to: (1) primary local acupoints ST2 (Sibai), ST7 (Xiaguan), and ST4 (Dicang) on the affected side; (2) branch-specific supplementary points GB1 (Tongziliao) for ophthalmic branch involvement, SI18 (Quanliao) for maxillary branch involvement, and ST6 (Jiache) for mandibular branch involvement; and (3) bilateral distal points LI4 (Hegu) and TE5 (Waiguan). Local acupoint pairs (ST7 adjacen

Первичные конечные точки

  • Changes in Visual Analog Scale (VAS) scores from baseline to the end of the 4th week of treatment [Срок оценки: Baseline, 4 weeks after treatment.]
Вторичные конечные точки (6)
  • Changes in Visual Analog Scale (VAS) scores [Срок оценки: Baseline, 2 weeks after treatment, at 4-week follow-up.]
  • Pain Diary Card [Срок оценки: Daily from enrollment through four weeks after treatment completion]
  • Carbamazepine Adverse Reactions [Срок оценки: Daily from enrollment through four weeks after treatment completion]
  • Hepatorenal function [Срок оценки: Baseline, 4 weeks after treatment.]
  • Changes in the The Self-Rating Anxiety Scale (SAS) [Срок оценки: Baseline, 2 weeks after treatment, 4 weeks after treatment, at 4-week follow-up.]
  • Changes in the Self-Rating Depression Scale (SDS) [Срок оценки: Baseline, 2 weeks after treatment, 4 weeks after treatment, at 4-week follow-up.]

Критерии участия

Критерии включения

  • Participants must meet all of the following criteria to be eligible for this study:
  • Met the diagnostic criteria for trigeminal neuralgia (TN) as defined in the International Classification of Headache Disorders, 3rd edition (ICHD-3) published by the International Headache Society (IHS) in 2018.
  • Between 18 and 75 years old (inclusive), regardless of gender;
  • Currently prescribed carbamazepine (400-800 mg/day) or oxcarbazepine (800-1600 mg/day);
  • Conscious, alert, and capable of perceiving/differentiating pain, with basic communication abilities;
  • Signed informed consent form and voluntary participation in the study.

Критерии исключения

  • Patients meeting any of the following criteria were excluded:
  • Patients with epilepsy, head injury, or other relevant neurological disorders;
  • Patients with severe cardiac, hepatic, or renal impairment;
  • Patients with cognitive dysfunction, aphasia, psychiatric disorders, or those unable to cooperate with treatment;
  • Patients with poorly controlled hypertension or hyperglycemia;
  • Patients with a recent diagnosis of severe anxiety or depression;
  • Pregnant or breastfeeding patients;
  • Patients with pacemakers or other contraindications to electroacupuncture;
  • Patients concurrently enrolled in other clinical studies.

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
Двойное слепое
Основная цель
Лечение

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07074561 · GZY-KJS-ZJ-2025-006-PSA

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗