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Perioperative Blood Pressure Screening to Improve Long-term Cardiovascular Health

NCT03634813 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2022-11-17

Study results available
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Summary

To explore in a pilot randomized clinical trial, the impact of Home Blood Pressure Monitoring with patient directed information as compared to usual care on the postoperative management of blood pressure.

Conditions

  • Blood Pressure

Interventions

DEVICE

High Blood Pressure Monitor

High Blood Pressure Monitoring device (Omron MX3 model BP742, Omron, Shaumberg, IL)

PROCEDURE

Usual Care

Usual Care

Sponsors & Collaborators

  • Yale University

    lead OTHER

Principal Investigators

  • Robert Schonberger, MD · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-31
Primary Completion
2020-05-01
Completion
2021-04-17
FDA Device
Yes

Countries

  • United States

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 NCT03634813 on ClinicalTrials.gov