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Clinical Study between Chavyadi churna sattu and Trayushnadi churna in the management of Sthoulya with special reference to Obesity.

Comparative Clinical Study to Evaluate Efficacy of Chavyadi churna sattu and Trayushnadi churna in the management of Sthoulya with special reference to Obesity. - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070898
Enrollment
60
Registered
2024-07-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E00-E89- Endocrine, nutritional and metabolic diseases

Interventions

None listed

Sponsors

Dr Pranita Bhavsar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients with BMI more than 30 will be enrolled for project 2)Subjects in the age group 20-70 years, both inclusive, male ,females 3) Uncomplicated new diabetes patients will be in inclusion 4) In trial apple shaped / pear shaped obese patient will be included 5) Patients with obesity suffering with weight bearing joint pain will be included 6) Subjects who are willing to give informed consent and ready to comply with the protocol will be included

Exclusion criteria

Exclusion criteria: 1)Subjects having any other major k/c/o.- IHD, CKD,HTN,Tb will be excluded 2)Patients with k/c/o cushings syndrome will be excluded 3) Patients on corticosteriods will be excluded 4) Known case of any active malignancy will be in exclusion criteria 5) Patient of chronic diabetes mallitus will be excluded 6) Patients with obesity class iii will be excluded 7) Known case of hypothyroidism will be excluded 8) Subjects having known chronic infectious disease , such as tb ,hep B , hep C will be excluded 9) Pregnancy and lactating mothers will be excluded 10) Patients with any disability will be excluded 11) Other conditions , which in the opinion of investigators , makes the patient unsuitable for enrollment or could interfere with his/her participation in the trial and completion of the protocol will be excluded

Design outcomes

Primary

MeasureTime frame
Relief in the subjective assessment crieteria i.e chalatva of spik stana and udara, sweda adhikatwa,nidra adhikya,atikshudha , atipipassa,angagaurava,gatrasada .Timepoint: follow up will be after 30days for 3months (90 days)

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Neena Damle

D.Y.Patil school of Ayurveda ,nerul ,navi mumbai

neena.damle@dypatil.edu7977153510

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026