CTRI/2018/05/013843Not yet recruitingPhase 4
Comparative clinical and ultrasonographic evaluation of the efficiency of Placentrex with Dexamethasone & Hyaluronidase with Dexamethasone in the treatment of Oral Submucous Fibrosis- A randomized Control Trial
Dr Sosa George0 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)Individuals clinically diagnosed with Oral Submucous Fibrosis with palpable bands in the oral cavity
- •2)OSMF patients with mouth opening greater than 25mm
- •3)Individuals with willingness to quit the habit that caused the disease
- •4)Individuals willingly consenting to take part in the study
- •5)No previous history of treatment for oral submucous fibrosis
- •6)no other concurrent oral lesions
Exclusion Criteria
- •1)Patients who are unwilling to quit the habit that caused the disease.
- •2)Patients unwilling to consent for the study.
- •3)Previously treated Oral Submucous Fibrosis.
- •4)Currently under treatment for Oral Submucous Fibrosis.
- •5)Presence of other concurrent oral premalignant lesions.
- •6)Health status which makes the patient not a feasible candidate for the trial.
Investigators
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