MedTrace Logo

PMP-300E (Smart Watch): Portable Monitoring Device Study

NCT01364740 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2017-01-27

Study results available
· View outcomes & findings →

Summary

Validation of Portable Monitoring Device PMP-300E for Identification of Obstructive Sleep Apnea.

Conditions

Interventions

DEVICE

PMP-300E

Data collected from Level 3 device

DEVICE

In-lab PSG

Data collected from Type I In-Lab Polysomnography

Sponsors & Collaborators

Principal Investigators

  • Clete A. Kushida M.D., Ph.D. · Stanford University

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2012-05-31
Completion
2012-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

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 NCT01364740 on ClinicalTrials.gov