CTRI/2025/01/079681Not yet recruitingPhase 2
A CLINICAL STUDY TO EVALUATE THE ANALGESIC EFFICACY OF SHOOLPRASHAMANAM MAHAKASHAYAM GHAN VATI ALONG WITH DASHMOOLA KWATH IN PAIN [SHOOL] MANAGEMENT OF AMAVATA (RHEUMATOID ARTHRITIS)
Pt khushilal sharma Government Autonomous colllege and institue bhopal mp1 site in 1 country40 target enrollmentStarted: February 15, 2025Last updated:
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 40
- Locations
- 1
- Primary Endpoint
- It is expected that at the end of the study, we would be able to demonstrate and explain the efficacy of Shoolprashamanam mahakashayam ghan vati along with Dashmoola kwath in the pain management of Amavat (RA).
Study Overview
Brief Summary
It is expected that at the end of the study we would be able to demonstrate and explain the efficacy of shoolprashamanam mahakashayam ghan vati along with Dashmoola kwath in the management of Amavata( rheumatois arthritis)
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- Participant Blinded
Eligibility Criteria
- Ages
- 26.00 Year(s) to 55.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Patient fulfilling the American college of Rheumatology revised criteria of RA.
- •Sign and symptoms of Amavata which are mention in our classics.
- •Patients willing and able to participate in the study and give written consent form.
Exclusion Criteria
- •patients below 26 year and above 55 years Patients who develop secondary complications of R.A. e.g. Pleuro-pericardial disease, severely damaged joint with bed ridden patients and severe joint and crippling deformity .
- •Patient having any other serious illness e.g. Hepatic/renal failure, severe GERD.
- •Patients with diagnosed other arthritis like Gouty arthritis, tuberculosis or psoriatic arthritis etc.
- •Immunocompromised patient, cancer, AIDS, heart disease, polycystic kidney disease.
- •Pt. who are not willing to give consent.
Outcomes
Primary Outcomes
It is expected that at the end of the study, we would be able to demonstrate and explain the efficacy of Shoolprashamanam mahakashayam ghan vati along with Dashmoola kwath in the pain management of Amavat (RA).
Time Frame: 12 months
Secondary Outcomes
- It is expected that at the end of the study, we would be able to manage pain intensity of Aamvata with Shoolprashmanam Mahakashyam ghan vati along with Dashmool kwath
Investigators
Dr urvashi chandrol
pt khushilal sharma gov Ayurvedic college bhopal mp
Study Sites (1)
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