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This study to evaluate the better therepy in between katibasti and abhyanga with dhatturadya tail in the treatment of katigraha or lumbar spondylosis

A comparative clinical study of katibasti and abhyanga with dhatturadya tail in the management of katigraha W.S.R. to lumbar spondylosis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/023850
Enrollment
60
Registered
2020-03-09
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M478- Other spondylosis

Interventions

Intervention1: nil: nil Control Intervention1: katibasti and abhyanga with with dhatturadya tail: group A- katibasti with dhatturadya tail for 30 minutes for 7 days group B- abhyanga with dhatturadya

Sponsors

Dr akanksha keshari
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. pt. will be selected fullfilling the criteria of katigraha (sym.- katigraha, katishoola, sakhti rja, supti). 2. pt. aged between 20-70 yrs. with irrespective of gender. 3. pt. with degenerative changes in X-RAY lumbar spine. 4. pt. willing to participate in trial.( consent duly filled).

Exclusion criteria

Exclusion criteria: 1. pt. aged less than 20 yrs. and more than 70 yrs. 2. pt. who are having any anatomical/congenital deformities and need surgical care. 3. conditions related to spine other than spondylosis will be excluded, e.g.- A.S.,SSA. 4. pt. having any other systemic major illness e.g.- cardiac disorders, C.R.F., diabetes, systemic lupus erythromatus, R.A., gout, T.B.etc will be excluded.

Design outcomes

Primary

MeasureTime frame
relief in katigraha relief in kati shoola relief in sakthi ruja relief in suptiTimepoint: 14 days

Secondary

MeasureTime frame
nilTimepoint: nil

Countries

India

Contacts

Public ContactDr A K Singh

hubhdeep Ayurved Medical College and Hospital

vaidyavyas@gmail.com9425092343

Outcome results

None listed

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