NCT00416299

Brief Summary

To evaluate the use of new cardiac biomarker for the prediction of in-hospital cardiovascular complications in elderly patients undergoing elective cardiac surgery.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started May 2007

Shorter than P25 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

First Submitted

Initial submission to the registry

December 26, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 27, 2006

Completed
4 months until next milestone

Study Start

First participant enrolled

May 1, 2007

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2007

Completed
Last Updated

January 30, 2009

Status Verified

January 1, 2009

First QC Date

December 26, 2006

Last Update Submit

January 29, 2009

Conditions

Cardiac Surgery

Keywords

Cardiac biomarkercardiac surgeryelderlypostoperative complicationsPatients aged 75 years or older undergoing cardiac surgery

Eligibility Criteria

Age75 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • patients aged 75 years or older undergoing elective cardiac surgery with CPB

You may not qualify if:

  • positive cardiac troponin T test within the week before surgery
  • patients undergoing emergent procedures
  • patients with preoperative mechanical cardiac support
  • patients undergoing hemodialysis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Anesthesiology and Intensive Care Medicine Klinikum Ludwigshafen

Ludwigshafen, 67063, Germany

Location

MeSH Terms

Conditions

Postoperative Complications

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Stefan W. Suttner, MD

    Klinikum Ludwigshafen

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

December 26, 2006

First Posted

December 27, 2006

Study Start

May 1, 2007

Study Completion

August 1, 2007

Last Updated

January 30, 2009

Record last verified: 2009-01

Locations

DE(1)