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Management of Sthaulya with Amrutadhya Guggulu And Life Style Modification

A Clinical Study On Sthaulya And Its Management With Life Style Modification And Amrutadhya Guggulu

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/06/019608
Enrollment
30
Registered
2019-06-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Intervention1: AMRUTADHYA GUGGULU: AMRUTADHYA GUGGULU WILL BE PREPARED AS DESCRIBED IN SHARANGDHAR SAMHITA VATI KALPANA DOSE -4 TAB THRICE A DAY(EACH TAB 500MG ) Control Intervention1: Placebo Group:

Sponsors

Government Akhandanand Ayurved College Bhadra Ahmedabad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: PATIENTS HAVING BMI MORE THAN 25 AND LESS THAN OR EQUAL TO 35 WILL BE TAKEN FOR THE STUDY PRE OBESE AND OBESE CLASS 1 ACCORDING TO WHO PATIENTS HAVING KRUCHHA VYAVAYATA DAURBALYA DAURGANDHYA SWEDABADHA KSHUDHATIMATRAM ETC

Exclusion criteria

Exclusion criteria: PATIENTS HAVING PULMONARY DISEASE CARDIAC DISEASE HTN MI FEMALE WHO ARE PLANNING FOR CONCEPTION WILL BE EXCLUDED PATIENTS HAVING BMI MORE THAN 35

Design outcomes

Primary

MeasureTime frame
RESULT WILL BE ASSESSED ON THE BASIS OF SIGN AND SYMPTOMS OF STHAULYATimepoint: 4 weeks—

Secondary

MeasureTime frame
NoneTimepoint: None—

Countries

India

Contacts

Public ContactRuksar I Piparvadiya

Government Akhandanand Ayurved College Ahmedabad

shaikhmustak542@gmail.com9824440708

Outcome results

None listed

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