CTRI/2024/02/062681Not yet recruitingPhase 4
Comparative evaluation of effectiveness of diclofenac sodium gel (3%) phonophoresis and piroxicam gel (0.5%) phonophoresis in management of temporomandibular disorders – a single blind, randomized controlled trial. - TMDS
Shruti Saryam0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1.Patients fulfilling the Diagnostic criteria for temporomandibular disorders
- •(DC/TMD) for Pain-Related temporomandibular disorders which include
- •Myalgia (Local myalgia, myofascial pain, and myofascial pain with referral}
- •and Arthralgia.
- •2.Recurrent and chronic history of pain
- •3.Pharmacologic washout of =72 hours for central analgesic, NSAIDS, and
- •antidepressants.
- •4.Patients who have given Informed consent.
Exclusion Criteria
- •1.Patients fulfilling the DC/TMD CRITERIA of Diagnostic Procedures for Pain Related temporomandibular disorder which include Headache attributed
- •to TMD, Disc derangement , Degenerative joint disease, Subluxation.
- •? Patients on analgesics or anti-inflammatory medication who are not
- •willing to discontinue
- •2.Patients on Physiotherapy /complementary and alternative medicine for
- •the same problem.
- •3.Patient giving previous history of allergy to diclofenac sodium and
- •piroxicam drugs.
- •4.Patients with cardiac pacemakers and implanted defibrillators
- •5.Patients with jaw Tumors , fractures
- •6.Systemically compromised patients
- •7.Pregnant females
- •8.Patient not willing to give informed consent.
Investigators
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