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.
Investigators
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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