MedPath

Trimada in the Management of Medoroga

Phase 2
Conditions
Health Condition 1: E782- Mixed hyperlipidemia
Registration Number
CTRI/2023/07/054809
Lead Sponsor
Government Ayurvedic College, Patiala
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients who will give written consent for the study.

2.Patients fulfiling the diagnostic criteria as per clinical performa.

3.Any one of the following:

a)Dyslipidemia in laboratory investigation.

b)Patients having raised BMI between 25-39.9kg/metre square

Exclusion Criteria

1. Persons who will not agree to give written consent for the study

2. Patients below the age of 18 years and 60 years above

3. Pregnancy and lactating mothers

4.Patients having history of severe cardiac diseases

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Subjective Parameter- Grading will be done with signs & symptoms of Dyslipidemia/Medoroga. <br/ ><br>Lipid profile, CBC, LFT, KFTTimepoint: After 45 days of intervention of Trimada Churan orally & 15 days after stopping of medicine.
Secondary Outcome Measures
NameTimeMethod
Subjective Parameter- Grading will be done with signs & symptoms of Dyslipidemia/Medoroga. <br/ ><br>Lipid profile, CBC, LFT, KFTTimepoint: After 45 days of intervention of Trimada Churan orally & 15 days after stopping of medicine.
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