CTRI/2015/01/005397
Recruiting
Phase 3
A randomized double blind controlled clinical trial of an Ayurvedic formulation for the prevention and management of coronary heart disease.
Department of Science Technology0 sites1,000 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Department of Science Technology
- Enrollment
- 1000
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Diagnosed cases of CHD consenting to participate in clinical drug trial program were included in the study.
- •These CHD patient showing dyslipidemia, atherosclerotic, ischemic changes, elevated homocysteine and inflammatory markers, concentration with certain psychological complaints mainly sleep disturbances were treated with test formulation.
- •The diagnosis of CHD patients were done on the basis of clinical as well as laboratory findings.
Exclusion Criteria
- •Patients suffering from chronic illness like T.B., Rheumatoid arthritis, diagnosed IHD cases; Type\-1 diabetic patients; Evidence of hypo or hyperthyroidism; Age above 75 years.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
A double-blind randomised controlled clinical trial of levosimendan vs dopexamine in septic shockISRCTN46862968Record Provided by the NHSTCT Register - 2006 Update - Department of Health20
Terminated
Phase 4
A clnical trIal comparing the effect of treatment with oral spironolactone compared with a placebo on the frequency and duration of atrIal fibrillation in patients with an implanted cardiac device in New Zealand.ACTRN12616001188426niversity of Otago150
Recruiting
Not Applicable
The Comparison between two method of minisurgical percutaneous dilated tracheostomyThe relationship between two methods of small throat surgery through the skin.IRCT20150107020592N8Masih Daneshvari Hospital66
Completed
Not Applicable
Randomized clinical trial of five adhesive systems in occlusal posterior restorationsISRCTN87835631niversity of Coimbra (Portugal)70
Completed
Not Applicable
Safety and performance of Neuromuscular Electrical Stimulation (NMES) with the Neurotech Vital device for the treatment of stress urinary incontinence (SUI)ISRCTN68358784Bio-Medical Research Ltd (Ireland)140