Withings Devices Follow-up Study - Hypertension

NCT06692413 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2026-02-19

No results posted yet for this study

Summary

The primary objective is to evaluate the accuracy to predict uncontrolled hypertension with Withings device data.

Conditions

Interventions

OTHER

Questionnaire

Users who consent to the study will receive a questionnaire every 3 months

Sponsors & Collaborators

  • Withings

    lead INDUSTRY

Principal Investigators

  • de Havenon, MD · Yale University School of Medicine, Dept of Neurology

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-11-01
Primary Completion
2024-11-01
Completion
2024-11-01

Countries

  • United States

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 NCT06692413 on ClinicalTrials.gov