Effect of Navaka guggulu and Rasanjana ghanvati in Sthaulya

Not yet recruiting

• Conditions: Disease of digestive system, unspecified,

• Registration Number: CTRI/2019/03/018149
• Lead Sponsor: Rishikul Campus

Brief Summary

The Study main purpose is to Compare and evaluate the clinical efficacy of Navaka guggulu and Rasanjana ghanvati in the management of sthaulya and Assessment will be done statistically.trail yet not to be completed.

Detailed Description

Not available

Study Timeline

• Study Start: 2019-03-25
• Last Update Posted: 2020-06-02

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• clinical signs and symptoms of sthaulya.
• bmi> 25kg/square meter.

Exclusion Criteria

• patient with hypothyroidism and cushing syndrome 2.
• patient with long term steroid treatment 3.
• patient with severe hypertension.
• patient with evidence of renal, hepatic and cardiac involvement 5.
• patient with DM.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It will be carried out at interval of 30 Days till completion of trial(90 days)	It will be carried out at interval of 30 Days till completion of trial(90 days) | 2. will be carried out before , during and after the treatment. | 3. Assessment will be done statistically. | 4. Any addition or exclusion may be included as per necessity of the study.
2. will be carried out before , during and after the treatment.	It will be carried out at interval of 30 Days till completion of trial(90 days) | 2. will be carried out before , during and after the treatment. | 3. Assessment will be done statistically. | 4. Any addition or exclusion may be included as per necessity of the study.
3. Assessment will be done statistically.	It will be carried out at interval of 30 Days till completion of trial(90 days) | 2. will be carried out before , during and after the treatment. | 3. Assessment will be done statistically. | 4. Any addition or exclusion may be included as per necessity of the study.
4. Any addition or exclusion may be included as per necessity of the study.	It will be carried out at interval of 30 Days till completion of trial(90 days) | 2. will be carried out before , during and after the treatment. | 3. Assessment will be done statistically. | 4. Any addition or exclusion may be included as per necessity of the study.

Secondary Outcome Measures

Name	Time	Method
exacaberation in signs and symptoms	1 month

Trial Locations

Locations (1)

OPD and IPD of Rishikul Govt. P.G. Ayurvedic College & Hospital, Haridwar; 🇮🇳 Hardwar, UTTARANCHAL, India

OPD and IPD of Rishikul Govt. P.G. Ayurvedic College & Hospital, Haridwar

🇮🇳Hardwar, UTTARANCHAL, India

julika

Principal investigator

09649911486

julikadang1993@gmail.com