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Clinical Trials/CTRI/2024/12/077950
CTRI/2024/12/077950
Completed
Phase 2/3

Comparative Clinical Study Of Efficacy Of Lumbar Traction With Agnikarma And Lumbar Traction In Management Of Grudhrasi With Reference To Sciatica

Department of Shalyatantra Shree Saptashrungi Ayurved Mahavidyalaya And Hospital1 site in 1 country76 target enrollmentStarted: December 22, 2024Last updated:

Overview

Phase
Phase 2/3
Status
Completed
Sponsor
Department of Shalyatantra Shree Saptashrungi Ayurved Mahavidyalaya And Hospital
Enrollment
76
Locations
1
Primary Endpoint
Reduce The Sign And Symptoms Of Grudhrasi

Overview

Brief Summary

OBJECTIVES:

1)Primary objective-

•  To Compare the efficacy Of Lumbar Traction With Agnikarma And Lumbar Traction Alone In Management Of Grudhrasi.

  1. secondary Objective-

•To study the Agnikarma in detail as per ayurvedic concept.

•To study  the lumbar traction in detail as per modern concept.

• To study the effect of lumbar traction and Agnikarma in Grudhrasi.

PARTICIPANT

38 number of patients of each group having age  between 25yr to 60yr suffering with sign and symptoms of Grudhrasi and meeting inclusion and exclusion criteria will be randomised  And selected for study from OPD AND IPD department of shalyatantra of Shree Saptashrungi Medical College and Hospital Nashik.

INTERVENTIONS-

38 Patient In group A selected for lumbar traction and Agnikarma

38 Patient in group B selected for Lumbar Traction

Primary Outcome :

Reduce the sign and symptoms of Grudhrasi.

Secondary outcome:

Provide long term relief and reduce recurrence of disability.

Treatment Duration : 7 Days

Follow Up :1th , 7th , 14th Days

Data Analysis :The Wilcoxon Signed Rank Test and Mann-Whitney U Test were used to analyze intra-group and inter-group differences. Both treatments showed significant symptom relief, with Agnikarma with Lumbar traction performing better in terms of overall percentage relief. Data will be analysed using appropriate statistical methods to compare the

effectiveness of the both intervension  group.

Ethical Considerations : The study will be conducted in accordence with ethical guidelines and with

informed consent from participents.

Study Design

Study Type
Interventional
Allocation
Other
Masking
None

Eligibility Criteria

Ages
25.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • A Patient With The Following Symptoms Of Grudhrasi.
  • Ruka Toda Stambha Spandana Saktikshepanigrah Patient With Positive S.L.R. Test.

Exclusion Criteria

  • Patient Under Age Of 25yr And Over Age Of 60yr .
  • Patient With Evidence Of Carcinogenicity -Recent History Of Trauma, Fracture, Impact To Lower Extremity And Spine.
  • people with spinal cord infection ,tuberculosis,bone cancer.
  • Diabetes,stoke,convulsion, uncontrolled HTN, Ischemic heart disease -Pregnancy.

Outcomes

Primary Outcomes

Reduce The Sign And Symptoms Of Grudhrasi

Time Frame: 7 days

Secondary Outcomes

  • To provide relief & reduce recurrence of disability.(14 days)

Investigators

Sponsor
Department of Shalyatantra Shree Saptashrungi Ayurved Mahavidyalaya And Hospital
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Vikas Udaybhan Gupta

Shree Saptashrungi Ayurved Mahavidyalaya

Study Sites (1)

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