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WBPS A Prospective, Method Comparison, Proof of Concept Study

NCT02934386 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2017-11-27

No results posted yet for this study

Summary

The study will evaluate the accuracy of BP measurements by a new algorithm to be embedded to the existing CE-marked WinPack device, compared to two reference devices (one oscillometric and one volume-clamp device), in healthy subjects and patients undergoing a standardized physical-activity hypertensive protocol.

Conditions

  • Blood Pressure

Interventions

DEVICE

WinMedical WinPack device

Sponsors & Collaborators

  • CSEM Centre Suisse d'Electronique et de Microtechnique SA - Recherche et Developpement

    lead INDUSTRY

Principal Investigators

  • Cyril Pellaton, Dr · HNE - Hôpital Neuchâtelois, Site de Pourtalès

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-10-31
Primary Completion
2017-03-31
Completion
2017-03-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02934386 on ClinicalTrials.gov