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Clinical evaluate of trayodashanga guggulu and sahacharadi kwatha with and without greeva basti in the management of greevasandhigata vata.

A randomized comparative clinical study to evaluate the efficacy of Trayodashanga Guggulu and Sahacharadi Kwatha with and without Greeva Basti in the management of Greevasandhigata Vata w.s.r. to Cervical Spondylosis.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/03/024226
Enrollment
40
Registered
2020-03-24
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: M479- Spondylosis, unspecified

Interventions

Intervention1: Group B: 20 Patients will be treated by Trayodashang Guggulu 2 tab. (each tab. of 500 mg) after meals twice a day. Sahacharadi Kwatha 40ml Kwatha orally once empty stomach in morning fo

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient willing to participate in trial. 2.The patients in the age group of 18 - 70 years of either sex. 3.The patients having clinical sign and symptoms of Greevasandhigata Vata w.s.r. to Cervical Spondylosis. 4.The patients having chronicity of disease less than 5 years. 5.The patients having radiological finding of Cervical Spondylosis.

Exclusion criteria

Exclusion criteria: 1.Recent cervical, spinal, or shoulder surgery or implanted instrumentation or previous surgery for cervical spondylotic myelopathy. 2.Patients with long term history of steroid and cytotoxic treatment. 3.Patients having concomitant illness like uncontrollable Hypertension, Diabetes Mellitus etc. 4.Patients with evidence of malignancy. 5.Patient participated in any clinical trial within last six months. 6.Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Relief in Shoola (pain) in patients suffering with Greevasandhigata Vata.Timepoint: 30 days

Secondary

MeasureTime frame
Improvement in Neck Disability Index.Timepoint: 30 days

Countries

India

Contacts

Public ContactDr Ashok Kumar

National Institute of Ayurveda

hari_mohan68@yahoo.co.in9461297017

Outcome results

None listed

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