A clinical trial to study and compare the effects of hyaluronidase, dexamethasone and their combination in patients with oral submucous fibrosis
Phase 4
Completed
- Conditions
- Health Condition 1: null- Oral submucous fibrosis
- Registration Number
- CTRI/2014/10/005155
- Lead Sponsor
- STATE BOARD OF MEDICAL RESEARCH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
Patients clinically diagnosed and histopathologically confirmed as OSF
Exclusion Criteria
Patients having severe systemic problems or pregnant ladies,
patients having history of drug allergy or hypersensitivity to hyaluronidase, dexamethasone or lignocaine,
a previous history of treatment for OSF or malignancy arising in OSF or patients unwilling for treatment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method