Feasibility Study: Sleuth Monitoring System

NCT00719277 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2009-05-05

No results posted yet for this study

Summary

The purpose of the study is to evaluate the safety and performance of the Sleuth Monitoring system.

Conditions

Interventions

DEVICE

Sleuth Implantable ECG Monitoring System

The study device provides monitoring only. It cannot provide intervention or treatment.

Sponsors & Collaborators

  • Transoma Medical

    lead INDUSTRY

Principal Investigators

  • Wim Stegink · Transoma Medical

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-12-31
Primary Completion
2009-07-31
Completion
2009-09-30

Countries

  • Panama

Study Locations

More Related Trials

Entities

Diseases

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 NCT00719277 on ClinicalTrials.gov