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octurnal Blood Pressure dipping re-establishment with Melatonin.

Not Applicable
Conditions
Health Condition 1: I10- Essential (primary) hypertension
Registration Number
CTRI/2020/04/024768
Lead Sponsor
Centre for integrative Medicine and Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patients diagnosed with Hypertension.

On stable antihypertensive medication for 6 weeks before trial enrollment.

Non-dipping Blood pressure profile (>= 10% dipping of blood pressure at night in comparison of day on mean arterial blood pressure): On Ambulatory blood pressure monitoring.

Exclusion Criteria

Patients with accelerated hypertension (Stage III).

Patients with secondary hypertension: Renal disease, Endocrinopathies.

Patients with history of target organ damage (Nephropathy, Retinopathy).

Patients with other cardiac disorders Example: Heart failure (EF <50%), congenital cardiac heart disease, atrial fibrillation infection.

Major Stroke or recent stroke.

Patients on the drug interacting with Melatonin.

Circadian rhythm sleep wake disorders (DSPS, ASPS, Shift workers)

No acute coronary syndrome (PCI and CABg) with in 3 Month.

Major depressive disorder on medication.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Establishment of dipping pattern (10% reduction in nocturnal blood pressure from than daytime) of blood pressure on ambulatory blood pressure monitoring.Timepoint: At 3 Months and 6 Months
Secondary Outcome Measures
NameTimeMethod
To compare re-establishment of dipping between melatonin and placebo according to prakriti type. <br/ ><br>Improvement in sleep qualityTimepoint: 6 months
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