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Clinical Trials/CTRI/2024/06/068426
CTRI/2024/06/068426
Not yet recruiting
Phase 3

A comparative controlled clinical study to evaluate the effect of Raktamokshana by Shringa and cupping method in the management of Katishoola with special reference to low back pain. - NI

Dr.Vipul Ajitkumar Gangwal0 sites0 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Dr.Vipul Ajitkumar Gangwal
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Dr.Vipul Ajitkumar Gangwal

Eligibility Criteria

Inclusion Criteria

  • Patients fulfilling the diagnostic criteria. • Duration not more than 6 weeks, • Patients of both gender aged between 16\-70 years. • Irrespective of sex age education for all category and socieo\-economical status. • Patient willing for trial and giving written consent. • Patient who will be comfortably able to complete the Raktamokshana in Sitting with elevated back and forward bending head or prone position.

Exclusion Criteria

  • Known Case of Any systemic disorder or any serious illness, maligancny, infectious disease , congenital problem, hypertension , HIV positive , HbsAg positive or Covid 19 positive patients, Any known case of Neuroloigcal disorders.
  • Patients who is pregnant will be excluded for Raktamokshana.
  • Patients is having any history of cardiac disorder or on any blood thinner medicine or known case of any heamtological disorders. • Patient having Hemoglobin percentage less than 12 for women and less than 13 for men. • Age less than 16 and beyond 70 will not be included in studies. • Earlier went to the Cupping therapy or Shringa therapy or Cupping therapy. • Patients having associated diseases like Tuberculosis, Fractures, and other complications. • Patients having marked deformities of spinal column. Such as Sacralisation Spinal stenosis, Disturbed bowel\-bladder control.

Outcomes

Primary Outcomes

Not specified

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