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A Comparative Clinical Study on Shunthiyadi Kwatha and Pashanabhedadi Kwatha in the Treatment of Kidney Stones (Mutrashmari)

A Randomized Comparative Clinical Study To Evaluate The Efficacy Of Shunthiyadi kwatha and Pashanabhedadi kwatha In Mutrashmari WSR Urolithiasis - Nil

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105922
Enrollment
60
Registered
2026-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: N209- Urinary calculus, unspecified

Interventions

None listed

Sponsors

National Institute of Ayurveda, Deemed To Be University,jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients Of Either Sex Male Or Female. 2. Patients Of Age Group From 18 to 60 Years. 3. Patient having renal and ureteric stones with Size Upto Less Than Or Equal To 10mm Will Be Include In This Trial .

Exclusion criteria

Exclusion criteria: 1.Age Below 18 Years And More Than 60 Years. 2.Patient With Obstructive Uropathy. 3.Patient With Chronic Kidney Diseases, Nephrotic Syndrome. 4.Patient With Hydronephrosis .(Grade3 And Grade4) Grade 3 (Moderate)- Moderate Dilation Of The Renal Pelvis And Calyces. Blunting Of Fornices And Flattening Of Papillae Mild Cortical Thinning May Be Seen. Grade 4 (severe)- Gross Dilation Of The Renal Pelvis And Caleyes, Which Appear Ballooned . Loss Of Border Between The Renal Pelvis And Calcyes. Renal Atrophy Seen As Cortical Thinning 5.Patient With Evidence Of Malignancy. 6.Patient With Poorly Controlled Diabetes Mellitus (HBA1C More Than 8%). 7.Pregnant Or Lactating Women. 8.Symptomatic Patients With Clinical Evidence Of Heart Failure. 9.Patient With Urolithiasis (Mutrashmari) With Complication, Such As AcutE Renal Failure, Sepsis, Anuria, Urinary Tract Infection With Renal Obsturction 10.Urinary Stones Of More Than 10mm Size. 11.Uncontrolled Hypertension (Systolic Blood Pressure More Than 160mmHg Or Diastolic Blood Pressure More Than 100 mmHg). 12.Presence Of Any Other Serious Medical Condition That May Interfere With Study Participation.

Design outcomes

Primary

MeasureTime frame
The Primary Outcome Of The Study Will Be Change In Size Of Renal Or Ureteric Calculus As Assessed By Ultrasonography (KUB),From Base Line To End Of The Treatment Period.Timepoint: Base Line To The End Of The Treatment Period

Secondary

MeasureTime frame
Secondary Outcome Will Include 1.Change In Clinical Symptoms Of Urolithiasis (Pain In Renal Angle And Loin Region,Radiating Toward The Groin, Burning Micturition, Dysuria, Hematuria, Nausea/Vomiting) 2. Change In Urine Microscopic Parameters (Pus Cells, RBCs, Urinary Crystals, Microbial Load). Safety Assessed By Monitoring Adverse Events. Timepoint: Baseline, Day 15, Day 30, and Day 45.

Countries

India

Contacts

Public ContactPROF HARI MOHAN LAL MEENA

National Institute of Ayurveda, Deemed to be university, Jaipur

hari_mohan68@yahoo.co.in9461297017

Outcome results

None listed

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