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A clinical study to evaluate tha effectiveness of masha taila through greeva basti and nasya karma along with rasnadi guggulu in the cases of cervical spodylosis

A clinical study to evaluate the effectiveness of masha taila through greeva basti and nasya karma along with rasnadi guggulu in the cases of greeva stambh w.s.r. cervical spodylosis - CSMGNRGCS

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032653
Enrollment
60
Registered
2021-04-08
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: Greeva Basti with mashataila,along with Rasnadi guggulu.: Group A- In this group patient will be treated with Greeva Basti with mashataila,along with Rasnadi guggulu orally for 3 months

Sponsors

State Ayurvedic College and Hospital Lucknow
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Griva Shool(Neck Pain), Griva Stambh (Stiffness of Neck), Griva Hundan (Restricted movement of Neck), Gatra Suptata (Paraesthesia), Paniprasthshiroruja (Rediation of Pain to back of Head, Shoulder and Arms), Anidra (Sleep Disturbance)

Exclusion criteria

Exclusion criteria: Patient below 26 years and above 65 years of age, extra cervical ribs, patient having injury to cervical spine, diabetic neuropathy, gouty & Rheumatoid Arthritis, Torticollis, Ankylosing Spondylitis

Design outcomes

Primary

MeasureTime frame
To compare the effectiveness of Masha Taila through Greeva Basti &Nasyakarma &along with RasnadiGugglu in cases of GreevaStambhw.s.r (Cervical Spondylosis)â??Timepoint: 90 days

Secondary

MeasureTime frame
ï?¼ To assess the effectiveness of trial drug in improving the condition of disease.Timepoint: 90 days

Countries

India

Contacts

Public Contactrekha bajpai

State Ayurvedic College and Hospital , lucknow

drsandeeprac@gmail.com8299597009

Outcome results

None listed

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