Clinical Validation of The Combei BP 880 W

NCT05883605 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 85

Last updated 2023-06-01

No results posted yet for this study

Summary

Clinical validation of the wrist blood pressure measuring device Combei BP 880 W for home use according to "the Universal Standard for the validation of blood pressure measuring devices by the Association for the Advancement of Medical Instrumentation/European Society of Hypertension/International Organization for Standardization (AAMI/ESH/ISO)" in the general population.

Conditions

Interventions

DEVICE

Measuring blood pressure

Measuring blood pressure using electronic device and using a mercury sphygmomanometer

Sponsors & Collaborators

  • International Society for Vascular Health

    lead OTHER

Principal Investigators

  • ROLAND ASMAR · International Society of Vascular Health

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-01-10
Primary Completion
2023-05-23
Completion
2023-05-27

Countries

  • France

Study Locations

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Entities

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 NCT05883605 on ClinicalTrials.gov