Hypertension Clinical Trial
Official title:
An Updated Wearable Magnetic Flux Device to Optimize Blood Pressure Control
The goal of this study involving a wearable magnetic flux device is to study the impact of static magnetic flux on blood pressure control in hypertensive and normotensive populations. The main objectives are: 1. Study the safety and efficacy of static magnetic flux on blood pressure control in normal and hypertensive patients. 2. Incorporate this into a portable, wearable device to increase availability and outreach. Participants will be required to wear a wearable BP device, an ambulatory BP and answer a questionnaire for this study. Researchers will compare between hypertensive and normotensive groups to achieve objective of this study.
Status | Recruiting |
Enrollment | 200 |
Est. completion date | April 30, 2024 |
Est. primary completion date | March 30, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 21 Years to 80 Years |
Eligibility | Inclusion Criteria: - For normotensive patients, Systolic Blood Pressure 100-139mmHg/ Diastolic Blood Pressure 50-89mmHg - For hypertensive patients, SBP 140-180mmHg, DBP 90-110mmHg (no change in blood pressure medications in last one month) OR Hypertensive patients with stable blood pressure (SBP not <100, DBP not <50) well controlled on medication Exclusion Criteria - SBP <100mmHg, DBP<50mmHg - SBP>180mmHg, DBP >110mmHg - Recent change (<1month) in blood pressure medications - Prior stroke - Prior ischemic heart disease - Prior peripheral vascular heart disease - Prior carotid stenosis or bruit - Presence of metallic implants (e.g. ICD, pacemaker, etc) - Pregnancy - Breast feeding - Allergy to device material/skin allergy |
Country | Name | City | State |
---|---|---|---|
Singapore | National Heart Centre Singapore | Singapore |
Lead Sponsor | Collaborator |
---|---|
National Heart Centre Singapore |
Singapore,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of blood pressure measurement after wearing study BP device | The investigators will be assessing the 24Hours ambulatory blood pressure monitor report with hourly averages to determine the outcome. Blood pressure measurements will reflect whether the wearable BP device has any impact on the participants' blood pressure before, during and after the participants wear the device. | 24 hours |
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