A clinical trial to find the efficacy and safety of â??Hypercumâ?? for the treatment of hypertensio
- Conditions
- Health Condition 1: I15- Secondary hypertension
- Registration Number
- CTRI/2012/09/003020
- Lead Sponsor
- MS Natural Solutions
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 16
•Males and females of age group 18-60 years
•Subjects who are willing to give written informed consent
•Patient running with Anti Hypertensive drugs or patient having known to be a Hypertensive patient but not yet approached any system of medication.
•Diabetic Patient or Patient running with Renal Failure or Patient having Metabolic Syndrome
•Female subjects who are confirmed as non-pregnant status and agree to comply with proper contraception throughout the study duration
•Patient is willing and able to comply with all trial requirements
•Severe essential hypertension
•Significant renal insufficiency [Serum Creatinine > 159 µmol/L ( > 1.8 mg/dl)]
•History of cerebro-vascular disease
•Patients with a history of HIV infection, AIDS, hepatitis B or C, or other immunosuppressive disorders
•Current diagnosis or a history of malignancy
•Drug of abuse within the past 2 years
•Pregnancy or breastfeeding
•Present history of mental diseases
•Previous participation in a clinical trial within 6 months
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method