CTRI/2024/04/065408尚未招募3 期
Comparing the effectiveness of Transcutaneous Electrical Nerve Stimulation (TENS) and Pilocarpine mouthwash with standard care on salivary flow in patients with radiation-induced xerostomia: a randomized controlled trial - NI
I0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Participants who meet the eligibility requirements for the study are those who have completed radiation therapy with or without chemotherapy or surgery between three months and two years prior to study entry, and who report symptoms of oral dryness and decreased salivary flow (= 0.2 mL/min).
- •All participants who are willing to give written informed consent.
排除标准
- •Participants with a history of known salivary gland pathologies, such as rheumatoid arthritis and Sjogrens syndrome.
- •Those who are taking drugs like pilocarpine, cevimeline, inhalatory glucocorticoids, opioids, benzodiazepines, diuretics, or who have undergone surgery involving the salivary glands.
- •Participants with hearing aids, cochlear implants, pacemakers or defibrillators will be excluded from the study.
- •Participants who have peptic ulcers or uncontrolled asthma will be excluded.
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