Effect of Modified Kati Basti in Katishoola

A Study to Design and Evaluate the Efficacy of Electronic Kati Basti Yantra In Katishoola- Randomized Controlled Clinical Trial - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/06/112746

Enrollment

Registered

2026-06-15

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-22

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

Conditions

Health Condition 1: M95-M95- Other disorders of the musculoskeletal system and connective tissue

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients between 20 to 60 years irrespective of gender will be considered. Patients with mechanical strain of musculoskeletal origin. Patients who are fit for Swedana. Patients who are willing to give consent.

Exclusion criteria

Exclusion criteria: Known case or clinical features suggesting sciatica, vertebral fracture, Lumbar spondylitis, Sacroiliitis. Traumatic and congenital deformities condition of the spine. Patients who are on Immuno-suppressants and steroids. Any surgical condition and skin diseases.

Design outcomes

Primary

Measure	Time frame
Restricted range of movement in Lumbar spine- assessed through Oswestry Disability Index and Schober s Test.Timepoint: 0th, 4th, 8th, 15th day	—

Secondary

Measure	Time frame
Functional assessment- assessed through Walking time, Climbing time.Timepoint: 0th, 4th, 8th, 15th day.	—

Countries

India

Contacts

Public ContactDr Shivaprasad Meti

Alvas Ayurveda Medical College

dr.rohiniayu@gmail.com9481845928

Outcome results