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Clinical Trials/CTRI/2025/09/094892
CTRI/2025/09/094892RecruitingPhase 3

Clinical evaluation of Shunthyadi kwath and Gokshuradi guggulu in Mutrashmari

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan1 site in 1 country30 target enrollmentStarted: October 1, 2025Last updated:

Trial Snapshot

Phase
Phase 3
Status
Recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
Subjective parameters.

Study Overview

Brief Summary

In this trial we are selecting patients of Mutraashmari  and take one  group of 30 patients . We will do intervention with standard  Shunthyadi kwath and Gokshuradai Guggulu . intervention  study to be done on the basis of assessment based on subjective and objective parameters. Subjective parameters includes Burning micturition , pain, dysuria , frequency of micturition , hematuria  and Objective parameters includes number of calculus , size of calculus  . Result will be analysed statistically and discussed accordingly .

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
18.00 Year(s) to 50.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients willing to undergo trial and ready to give informed and written consent Patients of both sexes and age group (18 to 50 yrs), irrespective of religion, socioeconomic status occupation will be taken Radiological evidence of (upto 8 mm) in kidney, ureter, urinary bladder & urethra.

Exclusion Criteria

  • Patients does not willing to undergo trial and ready to give informed and written consent. Complications related to Kidneys/ Ureter / Bladder like.
  • Acute Renal Failure, Chronic Renal Failure, Polycystic Kidney diseases, Impaired Renal function, etc. Other chronic diseases like TB (Tuberculosis), Hepatitis etc. will be excluded. Pregnant women and lactating mothers will be excluded. Patients will be dropped if they develop any complications during the course will also be excluded. Calculi size more than 8 mm. Patients having Moderate or severe Hydronephrosis will be excluded.

Outcomes

Primary Outcomes

Subjective parameters.

Time Frame: assessment will be done at baseline followed by every 4th week assessment until renal calculi completely removed

Pain

Time Frame: assessment will be done at baseline followed by every 4th week assessment until renal calculi completely removed

Burning micturition

Time Frame: assessment will be done at baseline followed by every 4th week assessment until renal calculi completely removed

Dysuria

Time Frame: assessment will be done at baseline followed by every 4th week assessment until renal calculi completely removed

Frequency of micturition

Time Frame: assessment will be done at baseline followed by every 4th week assessment until renal calculi completely removed

Hematuria

Time Frame: assessment will be done at baseline followed by every 4th week assessment until renal calculi completely removed

Secondary Outcomes

  • Subjective parameters.(Pain)

Investigators

Sponsor
Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Rekha

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan

Study Sites (1)

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