To see the effect of guduchi siddhaksheer ghrut in management of lumbar spondylosis when administered through rectal route.
- Conditions
- Osteoarthritis. Ayurveda Condition: SANDHIGATAVATAH,
- Registration Number
- CTRI/2025/05/086448
- Lead Sponsor
- Dr. Pratiksha Jaishankar Tripathi
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 45
- 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.
- 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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Katishoola 14 days
- Secondary Outcome Measures
Name Time Method Katistambha Akunchana Prasarana Pravrutti Savedana
Trial Locations
- Locations (1)
APMs Ayurved mahavidyala and seth R.V ayurved hospital sion
🇮🇳Mumbai, MAHARASHTRA, India
APMs Ayurved mahavidyala and seth R.V ayurved hospital sion🇮🇳Mumbai, MAHARASHTRA, IndiaDr Pratiksha Jaishankar TripathiPrincipal investigator8355803632drpratiksha.tripathi99@gmail.com