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Experimental study to assess the efficacy of Adityapaka Guggulu and Prasaranyadi Kwatha along with Anu taila Pratimarsha Nasya in the management of Greeva Sandhivata with special reference to Cervical Spondylosis.

Clinical study to evaluate the efficacy of Adityapaka Guggulu and Prasaranyadi Kwatha along with Anu taila Pratimarsha Nasya in the management of Greeva Sandhivata with special reference to Cervical Spondylosis.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/11/046954
Enrollment
66
Registered
2022-11-01
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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

None listed

Sponsors

Department of kayachikitsa Faculty of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients of either sex in the Age between- 20-60 yrs 2 Patients willing to participate for this trial with written informed consent obtained 3 Clinical symptoms of Greeva Sandhivata (Cervical Spondylosis)

Exclusion criteria

Exclusion criteria: 1 Myofacial pain syndrome 2 Patients suffering from any acute disease/any infectious disease /chronic disease/ Like RA, SLE etc 3 Patients suffering from neurodegenerative and post surgical conditions of cervical spine Myelopathy , stenosis of spinal canal 4 Patients with poorly controlled hypertension ( >140/90) 5 Patients with poorly controlled Diabetes mellitus having HbA1C of 7.5% 6 Patients who have a past history of any type of heart disease or stroke 7 Patient with any type of hepatic and renal disorder 8 Pregnant & lactating women

Design outcomes

Primary

MeasureTime frame
Relief in Cervical Pain (Sandhishoola) Sandhi shopha Vertigo Headache Tingling sensation NumbnessTimepoint: 2 months with a follow up of every 15 days

Secondary

MeasureTime frame
Assessment of - 1 Range of Motion 2 Laboratory parameters 3 X Ray Cervical SpineTimepoint: 2 months before and after trial

Countries

India

Contacts

Public ContactDr Shalini

Banaras Hindu University

dr.shalini@bhu.ac.in8114413534

Outcome results

None listed

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