Triphala Ghanavati in Sthaulya

Randomised open controlled clinical trial to evaluate the efficacy of Triphala Ghanavati in the management of Sthaulya w.s.r. to Obesity - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061988

Enrollment

Registered

2024-01-29

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

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

Conditions

Health Condition 1: E669- Obesity, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients having signs and symptoms of sthaulya Patients diagnosed with sthaulya Patient irrespective of caste income group occupation

Exclusion criteria

Exclusion criteria: Patient with clinical evidence of heart failure, serious hepatic disorder. Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
To study the efficacy of Triphala ghanvati in sthaulya w s r to obesity on assessment of subjective parameters such as angachalatva atipipasa atikshuda swedadhikya kshudraswasa dourgandyaTimepoint: 90 days	—

Secondary

Measure	Time frame
To asses the effect of Triphala ghanvati in signs & symptoms of sthaulya such as angachalatva atipipasa atikshuda swedadhikya kshudraswasa dourgandya To assess improvement by signs symptoms & gradation of assessment criteria To study etiopathology of sthaulya in detail according to ayurveda & obesity in detail according to modern text To improve quality of life & reduce discomfort of patient To achieve the outcome of study in 90 daysTimepoint: 90 days	—

Measure

Time frame

To asses the effect of Triphala ghanvati in signs & symptoms of sthaulya such as angachalatva atipipasa atikshuda swedadhikya kshudraswasa dourgandya To assess improvement by signs symptoms & gradation of assessment criteria To study etiopathology of sthaulya in detail according to ayurveda & obesity in detail according to modern text To improve quality of life & reduce discomfort of patient To achieve the outcome of study in 90 daysTimepoint: 90 days

—

Countries

India

Contacts

Public ContactDr Shivam Pramod Phopse

Yashwant Ayurvedic College Post Graduate Training and Research Centre Kodoli

drdipaliswamis@gmail.com9960003947

Outcome results