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

Comparative study on basti administered using modified basti putaka and enema can method in the management of vatakaphaja gridrasi. - Nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/11/060094

Enrollment

Registered

2023-11-21

Start date

Unknown

Completion date

Unknown

Last updated

2023-12-19

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

Conditions

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

Interventions

None listed

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

Measure	Time frame
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) 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 Timepoint: 3 Weeks 3 days	—

Measure

Time frame

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) 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 Timepoint: 3 Weeks 3 days

—

Secondary

Measure	Time frame
To asses the improvement in quality of lifeTimepoint: Improvement in the quality of life will be assesed for 7 days.	—

Countries

India

Contacts

Public ContactDrAshvini Kumar M

Department of Panchakarma Sri Dharmasthala Manjunatheswara college of Ayurveda and Hospital, Hassan

ashvinipanchakarma@gmail.com9448705660

Outcome results