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â??Role and effect of ayurvedic intervention in the management of Sandhigata Vata of Kati (Lumbar spondylosis)â??

â??A randomized controlled clinical trial to evaluate the efficacy of Ayurvedic intervention in the management of Sandhigatavata of Kati (Lumbar spondylosis)â??

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028631
Enrollment
100
Registered
2020-10-26
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: Rasnadashmooladi Kwatha Abhyanga, Swedana, Panchprasrutika Basti: Group B 50 patients will be performed Bahya Snehana, Swedana and Basti Karma for 15 days/month along with the trial dr

Sponsors

Central Council for Reasearch in Ayurvedic Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients willing for trial and give consent. 2.Patients of age group 30 to 60 years of either sex. 3.Patients having signs and symptoms of Sandhigatavata of Kati (lumbar spondylosis) as mentioned in Ayurvedic and Modern texts.

Exclusion criteria

Exclusion criteria: 1.Patients not willing for trial. 2.Age below 30 and above 60 years of either sex. 3.Patients having serious accidental injuries involving structural deformity. 4.Patients with Potts spine, spinal and paravertebral tumors. 5.Patients with fractures, kyphosis, scoliosis, osteoporosis 6.Patients with rectal or vaginal prolapsed, metastatic and uterine conditions. 7.Pregnant and lactating women. 8.Patients suffering from serious systemic disorders like renal diseases, heart diseases, malignant hypertention, diabetes mellitus.

Design outcomes

Primary

MeasureTime frame
Patients of both sexes between age group 30-60 of Sandhigata Vata of Kati Pradesh will be selected for relieving signs and symptomsTimepoint: 3 months

Secondary

MeasureTime frame
Assess the comparative efficacy between Ayurvedic intervention and Control group after 3 months in case of Sandhigatavata of Kati.Timepoint: 3 months

Countries

India

Contacts

Public ContactNiharika Shakya

Faculty of Ayurveda IMS Banaras Hindu University Varanasi

drjp98@yahoo.co.in9415814351

Outcome results

None listed

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