NCT01830023

Brief Summary

This study´s aim is to collect data of vitality diagnosis. A cardiac ultrasound examination will be done and the data will be compared to the other examinations.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,019

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2009

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2009

Completed
3.9 years until next milestone

First Submitted

Initial submission to the registry

April 9, 2013

Completed
2 days until next milestone

First Posted

Study publicly available on registry

April 11, 2013

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2013

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2013

Completed
Last Updated

September 23, 2015

Status Verified

September 1, 2015

Enrollment Period

4.3 years

First QC Date

April 9, 2013

Last Update Submit

September 22, 2015

Conditions

Cardiac Event

Keywords

cardiac ultrasoundvitalitydatapatientsexamined

Outcome Measures

Primary Outcomes (1)

  • vitality data

    1 day (at time of examination)

Study Arms (1)

cardiac ultrasound examination

Device: cardiac ultrasound examination

Interventions

cardiac ultrasound examinationDEVICE

cardiac ultrasound examination to examine the vitality

cardiac ultrasound examination

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients who are examined in the department of cardiology, university hospital Aachen

You may qualify if:

  • MRI exmination outcome: positive Late Enhancement, proof of infarction scars by contrast agent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Cardiology, university hospital

Aacehn, North Rhine Westfalia, 52074, Germany

Location

MeSH Terms

Conditions

Cardiovascular Diseases

Study Design

Study Type
observational
Observational Model
FAMILY BASED
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 9, 2013

First Posted

April 11, 2013

Study Start

May 1, 2009

Primary Completion

September 1, 2013

Study Completion

December 1, 2013

Last Updated

September 23, 2015

Record last verified: 2015-09

Locations

DE(1)