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Effect of Punarnavadi Kwath and Varunadi Kwath In The Management Of Mutravaha Sarotodushti ( Chronic Kidney Disesase )

Randomised Comparative Clinical Trial To Evaluate The Efficacy Of Punarnavadi Kwath And Varunadi Kwath In The Management Of Mutravaha Srotodushti W.S.R. Chronic Kidney Disease.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/033218
Enrollment
30
Registered
2021-04-28
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: N18- Chronic kidney disease (CKD)

Interventions

Intervention1: Punarnavadi kwatha: Orally Given Punarnavadi kwatha 40ml twice a day before meal for 30 days. Intervention2: Varunadi kwatha: 15 registered clinically diagnosed patients of Mutravaha

Sponsors

National Institute Ayurveda Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patient willing to participate in clinical trial 2 Patients having any clinical signs and symptoms of chronic renal failure 3 Patients with Hypertension 4 Patients of Serum creatinine level 1.2 to 5.0 mg/dl 5 Patients of Blood urea level 40 to 150 mg/dl

Exclusion criteria

Exclusion criteria: 1 Age: below 21 years and above 59 years 2 Patients having other associated disease like congenital disease Myeloma, Neoplasm etc. 3 Patient participated in any clinical trial with in last six months. 4 Pregnant or lactating women. 5 Familial or hereditary kidney disease, e.g. Polycystic kidney

Design outcomes

Primary

MeasureTime frame
Changes in the clinical symptoms of Mutravaha Srotodushti (Chronic Kidney Disease).Timepoint: 30 Days

Secondary

MeasureTime frame
Changes in the objective parameters.Timepoint: 30 Days

Countries

India

Contacts

Public ContactDr Karan Prakash Sharma

National Institute of Ayurveda

joshirk1964@gmail.com9414322297

Outcome results

None listed

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