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Clinical Trials/CTRI/2025/05/086448
CTRI/2025/05/086448Not yet recruitingPhase 4

A single-arm open-labelled clinical study to evaluate the efficacy of guduchi siddhaksheer ghrut basti in katisandhigata vata w.s.r. to lumbar spondylosis.

Dr. Pratiksha Jaishankar Tripathi1 site in 1 country45 target enrollmentStarted: May 17, 2025Last updated:
Conditions

Trial Snapshot

Phase
Phase 4
Status
Not yet recruiting
Sponsor
Enrollment
45
Locations
1
Primary Endpoint
Katishoola

Study Overview

Brief Summary

Nowadays humans are suffering from many lifestyle-related disorders due to the adaption of modern

lifestyle. Katisandhigata vata is one of them. It is not only clinical but also social, economic & public health

problems affecting the general population indiscriminately. It is not a life-threatening condition, but it

causes great discomfort and restriction in social and other activities [3]. 25% of females are prone to

Sandhigata Vata where whereas 16% of males are affected due to it. Conventional treatments, including

pharmacological interventions and physical therapy, often provide limited relief and may be associated with

side effects. Guduchi siddhaksheer ghrut basti, an ayurvedic therapeutic procedure involves the

administration of medicated Ksheerbasti prepared with guduchi. This study aims to evaluate the

effectiveness of guduchi siddhaksheer ghrut basti in managing symptoms of lumbar spondylosis, potentially

offering a holistic and safer alternative to conventional treatment.

Study Design

Study Type
Interventional
Allocation
Random Number Table
Masking
Not Applicable

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Patients having classical signs and symptoms of Katisandhigata Vata.
  • •(Niraam avastha) a.
  • •Katishoola (pain in low back) b.
  • •Katistambha (stiffness of lower back) c.
  • •Akunchana Prasarana Pravrutti Savedana (painful joint movements) Patients aged between 18 and 60 years and all genders.
  • •Diagnosed with lumbar spondylosis based on clinical and radiological finding.
  • •Willingness to participate and provide informed consent.

Exclusion Criteria

  • •Patients with acute lumbar spine injuries or fractures.
  • •Presence of systemic diseases such as diabetes, rheumatoid arthritis, CA, or any major autoimmune disorder Pregnant or lactating women.
  • •Patients not willing to consent.
  • •Patient not eligible for basti karma.

Outcomes

Primary Outcomes

Katishoola

Time Frame: 14 days

Secondary Outcomes

  • Katistambha(Akunchana Prasarana Pravrutti Savedana)

Investigators

Sponsor
Dr. Pratiksha Jaishankar Tripathi
Sponsor Class
Other [self]

Study Sites (1)

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