MedPath

AYURVEDIC MANAGEMENT OF NECK PAIN & STIFFNESS WITH "WARM MEDICATED OIL BATH" AND "MEDICATED PASTE" OVER NECK AREA.

Phase 1
Completed
Conditions
Spondylosis, unspecified,
Registration Number
CTRI/2018/10/016001
Lead Sponsor
National Institute Of Ayurveda
Brief Summary

Conclusion can be made from the present study that the symptomatic improvement in two groups, **Group-A***(Greeva Basti)*show Mild to Good improvement, while **Group-B** (*Greeva Lepan)* showed Mild to Moderate improvement in management of *Greevastambha.* On follow-up, relief was sustained for longer period in Group-A, as compared to Group-B.

Outof 15 patients in *Greeva Basti* Group(Group A) out of 15 patients,          07 (46.67%) patients showed moderate improvement,08 (53.33%) patient     showed good improvement in all symptoms after Treatment. Nopatient           remained unchanged and no patient felt Excellent improvement inGroup-A.Afterthe Follow up 02 (13.33%) patients showed mild improvement, 11 (73.33%) patientsshowed moderate improvement and 02 (13.33%) patients felt good improvement.

InGroup B out of 15 patients, 12 (80.00%) patients showed moderate improvement,03 (20%) patients showed good improvement after Treatment*.*

Afterthe Follow up 05 (33.33%) patients showed mild improvement, 10 (66.66%) patientsshowed moderate improvement. **From this data finally, we canconclude that *Greeva Basti* with *AshwagandhadyaTaila* is comparatively moreeffective and relief sustained for longer period as compared with *GreevaLepan* with *Vajigandha Kalka* but both modalitiesare effective in management of *Greevastambha* (Cervical Spondylosis) asthese are safe, cost effective and free from any adverse effects.**

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Patients suffering from classical signs and symptoms of Greeva stambha vis-a-vis cervical spondylosis.
  • Patients irrespective of sex, religion and socio-economic status.
  • Patient willing and able to participate in the study for 14 days.
Exclusion Criteria
  • Patients suffering from any acute diseases/ infectious diseases/metabolic diseases/chronic diseases (like rheumatoid Arthritis, DM, Gout, TB, SLE, Ankylosing spondylitis etc.) 2.
  • Patients with major systemic disorders that may interfere with the course of treatment.
  • Stenosis of Spinal Canal, Myelopathy.
  • Pregnant ladies and lactating mothers.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
improvement in Subjective and objective parameters.14 days
Secondary Outcome Measures
NameTimeMethod
To find the comparative efficacy of eithertreatment.

Trial Locations

Locations (1)

National Institute Of Ayurveda

🇮🇳

Jaipur, RAJASTHAN, India

National Institute Of Ayurveda
🇮🇳Jaipur, RAJASTHAN, India
DR GOPESH MANGAL
Principal investigator
8619849011
gmangal108@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.