Comparative Effect of Nigella Sativa and Conventional Management for OSMF
Oral Submucous Fibrosis

About this trial
This is an interventional treatment trial for Oral Submucous Fibrosis focused on measuring OSMF
Eligibility Criteria
Inclusion Criteria:
- Patients with the age of 18 years and above
- Patients clinically diagnosed with Oral submucous fibrosis
- Patients who have not received any treatment for Oral submucous fibrosis in the last three months.
- Patients who are willing to quit the habit of eating pan, gutka and areca nut
- Patients who are willing to attend the follow up visits
Exclusion Criteria:
- Patients who are less than 18 years of age
- Patients who are already using pain medications, corticosteroids or immunosuppressive drugs in any other form
- Patients with a history of malignancy
- Patients presenting with oral lesions other than Oral submucous fibrosis (OSMF)
- Patients who are allergic to the drug material used in the clinical trial
- Patients who will not give consent
Sites / Locations
- Ziauddin University, Clifton
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Steroid group
Nigella Sativa oil group
Participants in group 1 will be given corticosteroid lotion (Betamethasone valerate 0.1%) and will be advised to apply it topically (0.5 ml) on the buccal mucosa thrice a day along with physiotherapy using ice cream sticks three times a day for the duration of 10 minutes (3-5minutes on each side).
Group 2 will be given commercially available, cold pressed N.sativa (Black seed) oil and will be advised to apply it topically over the buccal mucosa (1 ml) thrice a day along with physiotherapy using ice cream sticks three times a day for the duration of 10 minutes (3-5minutes on each side).