Health Condition 1: I219- Acute myocardial infarction, unspecified
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adults of either gender ( 40 years older group) suffering from cardiovascular diseases (a narrow age range to avoid age-related circadian variations) 2. Cardiovascular disease diagnosed based on the clinical manifestations and confirmed through an electrocardiogram (ECG) 3. Age and gender (and occupation, if possible) matched healthy participants as control subjects based on medical history, clinical examination, and laboratory investigations 4. Subjects (patients and controls) willing to provide written informed consent and comply with protocol requirements
Exclusion criteria
Exclusion criteria: 1. Subjects reluctant to provide written informed consent or to comply with the study protocol 2. Subjects with any significant medical history (ongoing or in the recent past) 3. Currently diagnosed with a neurological or sleep disorder (narcolepsy, obstructive sleep apnea, restless leg syndrome) and/or being prescribed a non-psychotropic medication that can alter sleep and circadian rhythms (such as cortisone) 4. Subjects with severe anemia (Hb level < 7g/dL) 5. Female patients who are pregnant at the time of enrolment 6. Subjects who are chronic alcoholics or smokers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Altered rhythmicity of physiological and biochemical parameters in cardiovascular-diseased (CVD) patients.Timepoint: 3 years 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Optimal time of the day for beta-blocker administration in CVD patients.Timepoint: 3 years 6 months | — |
Countries
India
Contacts
Continental Hospital