Effect of two ayurvedic formulations in sthaulya

A clinical evaluation of (Kalpita) Agnimanthadi Kashaya and its comparative study with Varunadi Kashaya and Navaka Guggulu in Sthaulya in the purview of "Santarpanotthanamapatarpanamaushadham" - NIA/MS/2018/ANIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/03/023802

Enrollment

Registered

2020-03-06

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: Kalpita Agnimanthadi Kashaya: Dose 2 pala approx 100 ml, 50 ml morning and 50 ml evening in empty stomach, Dosage form Kashaya decoction, Mode of administration Oral, Duration 60 days C

Eligibility

Inclusion criteria

Inclusion criteria: Patient having clinical signs and symptoms of sthaulya as per classical ayurveda literature BMI above 30

Exclusion criteria

Exclusion criteria: Patients suffering from obesity due to hereditary indisposition Patients with hypothyroidism Patients suffering from drug induced obesity Patients with evidence of renal, hepatic and cardiac involvement Patients with diabetes mellitus Pregnant and lactating women Patients having disease for more than last 10 years BMI above 40

Design outcomes

Primary

Measure	Time frame
Effect of two therapies on BMITimepoint: 60 days	—

Secondary

Measure	Time frame
Effect of two therapies on body weight, lipid profile and classical symptoms of sthaulyaTimepoint: 60 days	—

Countries

India

Contacts

Public ContactKedar Lal Meena

National Institute of Ayurveda Jaipur

marvalanil@gmail.com6376589246

Outcome results

None listed

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