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Effect of Guduchyadi Yog With and Without Lifestyle Changes in the Management of Obesity

Comparative Clinical Evaluation of Guduchyadi Yog and Guduchyadi Yog with Lifestyle Modification in Sthoulya (Obesity) - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/111191
Enrollment
60
Registered
2026-05-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Sponsors

Shivani
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients between the age group of 18-50 years will be selected. 2. Patients having classical signs and symptoms of sthoulya (Sphika chalatva, Udara Chalatva, Stana Chalatva, Swaskasta, Janusandhi shool, Pipasaatiyogam, Swedadikyata, Daurgandhyam ,Daurbalya) 3. Patients between BMI of 25-40kg/m will be selected. 4.Patient having one or more than one levels among criteria according to National Cholesterol Eradication Programme ATP III

Exclusion criteria

Exclusion criteria: 1.Drug induced obesity. 2.Patients having serious diseases such as hepatic disease, cardiac disease, renal disease, pulmonary disease, history of thyroid, uncontrolled Hypertension and Diabetes mellitus, other endocrine disorders will be excluded. 3.Other systemic diseases which intervene with the course of treatment. 4.Patients having BMI more than 40kg/m will be excluded. 5.Patients with lipid profile values that exceed the upper limits specified in the inclusion criteria. 6.Pregnant females and lactating women will be excluded. 7.Patients who is unfit for Exercise.

Design outcomes

Primary

MeasureTime frame
Relief in Subjective parameters 1.Chalashphika udara stana 2.Alasya 3.Dourbalya 4.Swedaadhikya 5.Daurgandhyta 6.Kshudraswasa 7.Atinindra 8.AtipipasaTimepoint: Assessment will be done at baseline, then at 2nd week, then at 4th week ,then at 6th week, and then at the completion of trial at 8th week

Secondary

MeasureTime frame
Relief in objective parameters 1.Body weight 2.BMI 3.waist circumference 4.Hip circumference 5.Waist Hip ratio 6.Skin fold thickness 7.Lipid profileTimepoint: Assessment will be done at baseline, then at 2nd week, then at 4th week ,then at 6th week, and then at the completion of trial at 8th week

Countries

India

Contacts

Public ContactDr Abhishek Bhusan

Quadra Institute of Ayurveda and Hospital

ayu.abhishek@gmail.com9458636020

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026