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临床试验/CTRI/2024/06/068987
CTRI/2024/06/068987尚未招募4 期

Comparative assessment of efficacy of transcutaneous electrical nerve stimulation versus pharmacotherapy (drug combination of ibuprofen 400 mg, paracetamol 325 mg, chlorzoxazone 250 mg) in the treatment of patients with myofascial pain- A prospective randomised controlled trial. - NI

Dr Shah Nida Mujibur Rahman0 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
4 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

  • 1. Patients of either gender above 21 years of age.
  • 2. Patients having complaint of masticatory muscle pain.
  • 3. Pain and tenderness in the masticatory muscles on palpation.
  • 4. Patients who have not received any treatment for Myofascial pain, 3 months before the
  • research participation.

排除标准

  • 1. Pain of non-muscular origin (Dental, vascular or neural).
  • 2. Patients presenting with tenderness of temporomandibular joint on palpation.
  • 3. Completely edentulous patients or multiple missing teeth.
  • 4. Patients having epileptic attacks and seizures.
  • 5. Patients of known case of peptic ulcer.
  • 6. Patients mentally retarded or having neuromuscular problem.
  • 7. Patients on pacemakers, cochlear implants or metallic implants (as TENS can alter or adversely
  • affect the function of pacemakers).
  • 8. Patients with cardiac abnormalities (TENS can modify the cardiac impulse).
  • 9. Pregnant patients (TENS is contraindicated because it can cause preterm labour).
  • 10. Patients showing any allergy to lubricating gel used in TENS therapy.
  • 11. Patients with known allergy to chlorzoxazone, ibuprofen, paracetamol will be excluded.
  • 12. Patients who do not give informed consent will be excluded.

研究者

发起方
Dr Shah Nida Mujibur Rahman

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