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Comparison of Cuff-Less Wrist Wearable to Cuff Based Commercial Available Blood Pressure Measuring Devices in Health Volunteers With Normal or High Blood Pressure

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

(1) To compare cuff-less wrist wearable radial artery blood pressure measurements utilizing ViTrack(developed by Dynocardia) to the cuff based commercially available blood pressure device, in healthy volunteers with normal or high blood pressure.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

• Health volunteers 18 years and above; equal numbers of males and females to address Sex As a Biological Variable (SABV); and in sinus rhythm.

• Agree to commit to participate in the current protocol.

• Provide written informed consent prior to any study procedures being performed (all subjects should be able to understand the informed consent form and any other documents that subjects are required to read).

Locations
United States
Massachusetts
Dynocardia Inc
RECRUITING
Newton
Contact Information
Primary
Mohan Thanikachalam, MD
admin@dynocardia.care
+1 (617) 639 - 5569
Backup
Gokul Prasath Rajamanickam, MS
gokulpr@dynocardia.care
Time Frame
Start Date: 2021-01-01
Estimated Completion Date: 2026-11-30
Participants
Target number of participants: 91
Treatments
Experimental-Arm
For the same subject,~1. ViTrack wrist cuff is applied on one of the wrist~2. Standard Oscillometric cuff is applied to the brachial artery / wrist of the same arm~3. Auscultatory cuff is applied to the brachial artery of the same arm
Related Therapeutic Areas
Sponsors
Leads: Dynocardia, Inc

This content was sourced from clinicaltrials.gov