Comparative Study of Shatavari Ghrita in management of Lower Urinary Tract Infections.
- Conditions
- Cystitis, unspecified. Ayurveda Condition: PITTAJAMUTRAKRUCCRAM,
- Registration Number
- CTRI/2023/08/057085
- Lead Sponsor
- Government P.G. Ayurvedic college and Hospital, Varanasi
- Brief Summary
This study is Randomized, Parallel group study trial comparing the efficacy of Shatavari Ghrita Uttar Vasti and Snehapana in the management of Pittaja Mutrakrichhra (Cystitis).
Patients will be selected randomly from OPD and IPD of Department of Kayachikitsa and Panchakarma, Government P.G. Ayurvedic College and Hospital, Varanasi.
A total no. of 60 patients will be studied under two groups having 30 patients in each group-
Group A: In this group, 30 patients will be treated with Shatavari Ghrita Uttar Vasti for 7 days.
Group B: In this group, 30 patients will be treated with Shatavari Ghrita Snehapana for 7 days.
Two follow ups will be done- First on completion of treatment i.e. on 7th day and Second follow up on 15th day in each group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 60
- Patients are selected irrespective of Sex, Occupation, Caste, etc.
- Patients with signs and symptoms of Pittaja Mutrakrichhra as- Raktayukta, Shulayukta, Dahayukta, Krichh- Muhurmuhur Mutrapravartti, etc are included.
- Patients present with Pittaja mutrakrichhra as a primary complaint.
- Patient with recurrent cystitis.
- Patient below age of 16 years and above 60 years.
- Patient associated with Systemic chronic illness such as- Uncontrolled Diabetes, Acute Renal Failure, Chronic Renal Failure, Chronic Cystitis, Benign Prostate Hyperplasia, etc.
- Pregnant women.
- Renal calculus, Obstructive Uropathy, Poly Cystic Kidney Diseases, Glomerulo- nephritis, Nephrotic Syndrome, Urethral structure, etc.
- STDs, PIDs, etc.
- Cystitis as a complication of other diseases and as associated symptom of other diseases.
- Patients in whom Snehpana is contraindicated.
- Patients with raised lipid profile.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Relief in pain & burning sensation while micturation 3 days
- Secondary Outcome Measures
Name Time Method complete resolution of pain & burning micturition 15 days
Trial Locations
- Locations (1)
Government P.G. Ayurvedic college and Hospital, Varanasi
🇮🇳Varanasi, UTTAR PRADESH, India
Government P.G. Ayurvedic college and Hospital, Varanasi🇮🇳Varanasi, UTTAR PRADESH, IndiaDr Neha ChaudharyPrincipal investigator8318986643drnehachaudhary7@gmail.com