A CLINICO COMPARATIVE STUDY OF SHIROVIRECHANA PURVAKA KARNADHUPANA AND KARNADHUPANA ALONG WITH PATOLADI KWATHA IN THE MANAGEMENT OF KARNASRAVA (OTITIS MEDIA)
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- All the signs and symptoms of Karnasrava will be assigned score depending upon their severity to assess the effect of the drugs at the time, before and after the treatment.
Study Overview
Brief Summary
Aim of the study is to compair the efficacy of Shirovirechana purvaka Karnadhupana and Karnadhupana, along with Patoladi Kwatha in management of Karnasrava(Otitis Media). The study is randomized and patient selection will be blinded. Shirovirechana will be given for 7 days acconding to shashtrokta procedure and Karnadhupana will be given for 10 days and karnadhupana yantra will be made for that. Patoladi kwatha will be given for 30 days for shamana purpose.
Study Design
- Study Type
- Interventional
- Allocation
- Coin toss, Lottery, toss of dice, shuffling cards etc
- Masking
- Participant Blinded
Eligibility Criteria
- Ages
- 12.00 Year(s) to 80.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patients who are fulfilling the diagnostic criteria based on sign and symptoms of Karnasrava and indicated for shirovirechana will be selected.
Exclusion Criteria
- •Malignenecy, HIV, etc.and Patients having disease like Otitis Media, Eczematous Otitis Externa, Furunculosis in ear,Fungal infection, Granuloma,Polyp in ear,First and Second stage of A.O.M. and attico antral type of C.S.O.M. will be excluded.
Outcomes
Primary Outcomes
All the signs and symptoms of Karnasrava will be assigned score depending upon their severity to assess the effect of the drugs at the time, before and after the treatment.
Time Frame: All the signs and symptoms of Karnasrava will be assigned score depending upon their severity to assess the effect of the drugs at the time, before and after the treatment.
Secondary Outcomes
- All the signs and symptoms of Karnasrava will be assigned score depending upon their severity to assess the effect of the drugs at the time, before and after the treatment.(37 days)