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Clinical Trials/CTRI/2024/06/068987
CTRI/2024/06/068987
Not yet recruiting
Phase 4

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 sites0 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Dr Shah Nida Mujibur Rahman
Status
Not yet recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Dr Shah Nida Mujibur Rahman

Eligibility Criteria

Inclusion Criteria

  • •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.

Exclusion Criteria

  • •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).

Outcomes

Primary Outcomes

Not specified

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