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To study the effect of vidari kand in pittaja mitrakruchha an ayurvedic disease similar to urinary tract infection

Single Arm Clinical Study To Assess The Efficacy Of Vidari Kand Kwath In The Management Of Pittaja Mutrakruchha With Special Reference To Urinary Tract Infection - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086719
Enrollment
50
Registered
2025-05-13
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: N390- Urinary tract infection, site notspecified

Interventions

None listed

Sponsors

Sharik Manjur Mulla
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient having sign and symptoms of Pittaja Mutrakruchha as per Ayurvedic samhita will be randomly selected . Urine pus cells more than 5 / hpf. RBCs in urine more than 4 / hpf. Symptoms started within 15 days of period. 3 or more symptoms of urinary tract infection from following symptoms and presence of pus cells or RBC (25) Dysuria Macrohematuria Nycturia Suprapubic pain Incontinence over urine Offensive or foul smell

Exclusion criteria

Exclusion criteria: Patient with diabetes mellitus. Patients with known case of any systemic disease or urinary calculi. Patient with surgical history of any part of urinary tract. Patients with catheter related urinary tract infection. If crystals in urine are present.

Design outcomes

Primary

MeasureTime frame
To see effectiveness of vidari kand kwath in management of pittaja mutrakruchhaTimepoint: 15 days

Secondary

MeasureTime frame
To observe any adverse effect of vidari kamd kwath in patients of urianry tract infectionTimepoint: 15 days

Countries

India

Contacts

Public ContactDr Abhinandan Patil

LRP Ayurvedic medical college and hospital PG Institute and Research center Urun Islampur Sangli

drabhinandanpatil@gmail.com9890205000

Outcome results

None listed

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