NCT01100710

Brief Summary

The purpose of this study is to determine the influence of functional or anatomic cardiac parameters, age and gender on high sensitivity cTnT (TnThs) levels in healthy individuals.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
116

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Mar 2007

Typical duration 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

March 1, 2007

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2007

Completed
2.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2009

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 8, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

April 9, 2010

Completed
Last Updated

April 9, 2010

Status Verified

February 1, 2007

Enrollment Period

Same day

First QC Date

April 8, 2010

Last Update Submit

April 8, 2010

Conditions

Heart Failure

Keywords

Age Gender left ventricular mass high sensitive Troponin T

Study Arms (1)

healthy volunteers

Eligibility Criteria

Age20 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

residents of Heidelberg and urban hinterland

You may qualify if:

  • agreement, age \> 18 years, men and women

You may not qualify if:

  • measurable heart disease, any chronic or acute disease, intake of meds, hypertension, Diabetes

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital of Heidelberg

Heidelberg, Baden-Würtemberg, 69120, Germany

Location

Related Publications (1)

  • Apple FS, Smith SW, Pearce LA, Ler R, Murakami MM, Benoit MO, Levy C, Dumas C, Paul JL. Use of the bioMerieux VIDAS troponin I ultra assay for the diagnosis of myocardial infarction and detection of adverse events in patients presenting with symptoms suggestive of acute coronary syndrome. Clin Chim Acta. 2008 Apr;390(1-2):72-5. doi: 10.1016/j.cca.2007.12.016. Epub 2008 Jan 11.

    PMID: 18230357BACKGROUND

MeSH Terms

Conditions

Heart Failure

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Evangelos Giannitsis, Prof.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

April 8, 2010

First Posted

April 9, 2010

Study Start

March 1, 2007

Primary Completion

March 1, 2007

Study Completion

December 1, 2009

Last Updated

April 9, 2010

Record last verified: 2007-02

Locations

DE(1)