Clinical Trial To Study The Role Of Sontha Dhaniya Decoction And Boiled Water In Comparison To Normal Water Along With Some Ayurvedic Lifestyle On Weight Among Persons With Prodromal Symptoms Of Prameha (Prediabetes)

A Randomised Controlled Clinical Trial To Evaluate The Effect Of Sunthi Dhanyak Sadhita Jala And Ushnodaka As Compared To Normal Water Along With Comprehensive Ayurvedic Lifestyle Intervention On Weight Among Individuals With Prameha Purvaroopa (Prediabetes)

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/02/040617

Enrollment

114

Registered

2022-02-25

Start date

Unknown

Completion date

Unknown

Last updated

2024-11-11

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

Conditions

Health Condition 1: R739- Hyperglycemia, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: - Middle class family having RO purifier - Overweight and obese (BMI 23.0-29.9 kg/m2) - Any Sign/ symptoms of Prameha Purvaroopa as per classics along with HbA1C (5.7 to 6.4%) - Willing to participate and able to comply the study procedures and willing to give written informed consent.

Exclusion criteria

Exclusion criteria: - Pregnancy - Lactating mothers - Gestational diabetes - Diabetic case (patients on oral hypoglycaemic drugs or insulin) - Tuberculosis - Chronic kidney disease - Chronic Heart diseases - Chronic liver disease - Chronic obstructive pulmonary disease - Malignancies - Undergone any surgery within 2 months - Not willing to participate. - Any other criteria or major illnesses that investigator find inappropriate for the study will not be taken.

Design outcomes

Primary

Measure	Time frame
Change in weight of the patientsTimepoint: at baseline and every 15 days of follow up till 3 months of intervention	—

Secondary

Measure	Time frame
Changes in HbA1c, Lipid profile, TFT and Changes in quality of life via SF-36 questionnaireTimepoint: investigations and QOL at baseline and after 3 months on trial completion.	—

Countries

India

Contacts

Public ContactDR SHALINI RAI

All India institute of Ayurveda

drmoreanand@gmail.com9422025732

Outcome results