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A clinical study to see the effect of Ayyrvedic drug in the management of mukhroga

"A randomized comparative clinical study on the efficacy of daarvyadi qwath gandush and darvi raskriya pratisaran in the management of tridoshaja sarvasara mukhroga w.s.r to oral submucous fibrosis."

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021644
Enrollment
60
Registered
2019-10-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue

Interventions

Intervention1: Darvyadi kwathb gandush: Gandush 20-25 ml twice daily for 2 months Control Intervention1: Darvi Raskriya Pratisarana: Raskriya Pratisaran 3-6 gms twice a day for 2 months

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 to 60 years Patient having specific symptoms of Tridoshaja sarvasara Mukha roga Patient of either sex will be selected randomly

Exclusion criteria

Exclusion criteria: Individuals above 60 years and below 18years of age of either sex Extensive fibrosis with an inter incisal distance IID Premalignant and malignant changes Oral lichen planus Chronic debilitating conditions such as DM HT HIV etc Patients not willing to give up addiction habits of gutka ,panmasala tobacco and other narcotics

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of Darvyadi qwath gandush and darvi Raskriya pratisarana in the management of Tridoshaja Mukhroga ( Oral submucous fibrosis)Timepoint: 60 days—

Secondary

MeasureTime frame
Any adverse event reported voluntarily observed or enquired Recurrence in signs and symptoms of sarvasara mukhrogaTimepoint: 2 months—

Countries

India

Contacts

Public ContactDr Shamsa Fiaz

National Institute of Ayurveda

shamsa_fiaz@yahoo.com8764009846

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026