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Идёт набор NCT06548711

Effect of Transcutaneous Acupoint Electrical Stimulation (TAES) on Postoperative Cough in Lung Cancer

Без фазы С лечением Postoperative Cough Lung Cancer

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: Transcutaneous Acupoint Electrical Stimulation (TAES).
Кому может быть актуально
Состояния в реестре: Postoperative Cough, Lung Cancer. Базовые параметры: 18 лет — 80 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
Китай
Следующий шаг
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Официальное название

Director of Oncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

Обзор

Observation and exploration of the improvement in cough symptoms in postoperative lung cancer patients with Transcutaneous Acupoint Electrical Stimulation (TAES), the change in Cough Symptom Score (CSS) compared to baseline, the change in Visual Analog Scale (VAS) score for cough symptoms compared to baseline, the change in total score of Leicester Cough Questionnaire-Mandarin Chinese version (LCQ-MC) compared to baseline, and overall evaluation of treatment effectiveness by patients. A total of 84 postoperative lung cancer patients with cough were strictly selected according to the inclusion/exclusion criteria and treated and followed up according to the research plan requirements. Clinical observation forms were completed and clinical data were recorded in the database. Statistical analysis was performed on relevant clinical observation indicators to report research results and write related papers.

Подробное описание

To obtain sufficient evidence from evidence-based medicine, prospective, random, blind, and controlled clinical trials are adopted to evaluate the effectiveness and safety of TEAS in treating postoperative cough in lung cancer patients. This study aims to provide a potential non-pharmacological treatment option for postoperative cough patients with lung cancer, improve the quality of life of postoperative lung cancer patients, identify the population that is more likely to benefit from TEAS treatment and provide a solid scientific basis and guidance for personalized acupuncture treatment for postoperative cough in lung cancer patients.

Вмешательства

  • Другое Transcutaneous Acupoint Electrical Stimulation (TAES)
    Transcutaneous acupoint electrical stimulation (TAES) is a non-invasive treatment method that delivers gentle electrical pulses through the skin to specific acupuncture points on the body. This technique aims to mimic the effects of traditional acupuncture, providing a convenient and painless method of treatment.

Первичные конечные точки

  • LCQ-MC [Срок оценки: Prior to treatment (baseline), at the end of treatment (week 2), and 2 weeks after the end of treatment (week 4)]

Критерии участия

Критерии включения

  • Age between 18 and 80 years old - Surgery performed under general anesthesia for radical resection of lung cancer or lung cancer resection combined with lymph node dissection.
  • Pathological confirmation of primary lung cancer after surgery.
  • Duration of persistent dry cough after lung surgery ≥2 weeks.
  • Consciousness, ability to express opinions clearly, and voluntary signing of informed consent.

Критерии исключения

  • Patients diagnosed with acute respiratory system diseases within 1 month.
  • Patients diagnosed with pneumonia based on chest X-ray.
  • Patients with a history of asthma or tuberculosis.
  • Patients with uncontrolled hyperthyroidism, severe hypertension, heart disease, systemic infection, coagulation disorders (hypercoagulable state or bleeding tendency), or other severe systemic diseases.
  • Patients who have used steroid drugs within the past 3 months.
  • Patients who have taken angiotensin-converting enzyme inhibitors (ACEIs) within the past 6 months.
  • Patients with surgical incisions, skin allergies, wounds, or infections in the treatment area.
  • Patients who cannot tolerate transcutaneous acupoint electrical stimulation or withdraw during the procedure.
  • Patients with contraindications to transcutaneous electrical stimulation or implanted electrophysiological devices.
  • Patients who are pregnant or breastfeeding.

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

Китай · 1 центр
  • First Teaching Hospital of Tianjin University of Traditional Chinese Medicine — Тяньцзинь

Идентификаторы

NCT: NCT06548711 · TYLL2024[Z]026

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗