A clinical trial to study the effect of basti administered using modified basti putaka and enema can method in the management of vatakaphaja gridrasi.

Phase 3

Conditions: Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue

Registration Number: CTRI/2023/11/060094

Lead Sponsor: Sri Dharmasthala Manjunatheshwara College Of Ayurveda and Hospital Hassan

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Yet Recruiting

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

1)Participants full filling the diagnostic criteria

2)Participants fit for Basti Karma

3)Participants who are willing to participate and sign the informed consent form.

4)Participants with positive Straight Leg Raising (SLR) test

Exclusion Criteria

1)Pregnancy.

2)Uncontrolled Type 1 & 2 Diabetes mellitus & Hypertension.

3)Diagnosed cases of systemic disorders like chronic heart disease, chronic renal failure and chronic liver disease which may interfere with the course of the treatment.

4)History of HIV, HBsAg, Carcinoma and Tuberculosis.

5)Fractures of pelvis and femur.

6)Any conditions which investigators thinks may jeoparadise the study.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Samyak Basti Lakshanas,Basti peedana kala, Retention time of basti dravya and No of vegas will be assesed before and after treatment for two groups(Group A Modified Basti putaka and GroupB Basti Can method) <br/ ><br>Signs and symptoms of Gridrasi will be assesed with subjective parametrs like Ruk,Stamba,Toda,Aruchi,Gourava, Tandra and objective parameters like SLR, Range of movement before and after treatment <br/ ><br> <br/ ><br>Timepoint: 3 Weeks 3 days

Secondary Outcome Measures