CTRI/2025/09/094430Not yet recruitingPhase 2
An Exploratory Study To Compare The Effect Of Madhudaka And Triyushnadi Mantha In The Management Of Atisthoulya (Obesity)
PREETI CHAUHAN1 site in 1 country60 target enrollmentStarted: December 18, 2025Last updated:
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- REDUCTION IN SIGN AND SYMPTOMS OF ATISTHOULYA BY DECREASING BMI BREATHLESSNESS SNORING
Study Overview
Brief Summary
AN EXPLORATRY STUDY WILL BE DONE ON TWO GROUPS EACH CONSISTING 30 PATIENTS. ONE GROUP WILL BE ADMINISTERED MADHUDAKA IN QUANTITY OF 2 PAL OR 96GMS O.D. AND OTHER GROUP WILL BE ADMINISTERED TRIYUSHNADI MANTHA IN QUANTITY OF 2 PAL OR 96GMS O.D. FOR 45 DAYS. THEN PATIENTS WILL BE ASSESS BEFORE AND AFTER THE TRIAL ON THE BASIS OF SUBJECTIVE AND OBJECTIVE CRITERIA OF ATISTHOULYA AND FOLLOW UP WILL BE DONE EVERY 15TH DAY. THE DATA WILL BE COLLECTED AND ANALYZED STATISTICALLY USING APPROPRIATE TESTS.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Masking
- None
Eligibility Criteria
- Ages
- 16.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •The Patient Age Between 16-65 Years Irrespective Of Their Caste, Race And Sex Etc.
- •BMI Greater Than 25 And Above.
- •The Patient Having Clinical Signs & Symptoms Of Obesity.
- •The Patient Should Not Be On Any Other Medicine For Atisthoulya.
Exclusion Criteria
- •Patient With Endocrinal Disorder (D.M.) And Other Systemic Disease.
- •Patient With Long Term Steroid Treatment.
- •The Patient Having Obesity With Secondary In Origin.
- •Pregnant Women Drug Induced Obesity.
- •Patient Who Has BMI Less Then 25.
Outcomes
Primary Outcomes
REDUCTION IN SIGN AND SYMPTOMS OF ATISTHOULYA BY DECREASING BMI BREATHLESSNESS SNORING
Time Frame: SIX WEEKS
Secondary Outcomes
- IMPROVEMENT IN SUBJECTIVE AND OBJECTIVE ASSESSMENT CRITERIA OF ATISTHOULYA SUCH AS LESSER BMI(45 DAYS)
Investigators
DR SAURABH AGARWAL
PGIA JODHPUR
Study Sites (1)
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