Prokinecitine in Acute Myocardial Infarction (Prok-Idm)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified December 2013 by University Hospital, Strasbourg, France.
Recruitment status was:  Recruiting
Information provided by (Responsible Party):
University Hospital, Strasbourg, France Identifier:
First received: December 19, 2013
Last updated: NA
Last verified: December 2013
History: No changes posted
The study aims to investigate the presence of a substance in the blood called prokinecitine, which is released by the heart when a heart attack occurs. Several venous blood samples at the arm are withdrawn at admission, H6, H12, H24, H48 and H72 in order to measure the concentration of this substance in the blood. The usefulness of this new blood marker is going to be determsined to seek if it would be of help to better diagnose or estimate the gravity of heart infarction after a heart attack.

ST Elevatation Myocardial Infarction (STEMI)

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Pilot Study Prok-Idm: Interest of Dosage of Prokinecitine in Acute Myocardial Infarction

Resource links provided by NLM:

Further study details as provided by University Hospital, Strasbourg, France:

Primary Outcome Measures:
  • Infarct size by MRI necrotic myocardial mass [ Time Frame: 7 days ]
    Infarct size by MRI necrotic myocardial mass

Estimated Enrollment: 200
Study Start Date: November 2013
Estimated Study Completion Date: November 2016
Estimated Primary Completion Date: November 2016 (Final data collection date for primary outcome measure)

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with acute St elevation myocardial infarction of less than 6 hours

Inclusion Criteria:

  • Patients with acute St elevation myocardial infarction of less than 6 hours
  • Age>18 y/o

Exclusion Criteria:

  • Previous myocardial infarction
  • LBB, RBB
  • Renal Insuffiency MDRD<30 mL/min
  • Patient with Pace-Maker or ICD.
  Contacts and Locations
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Please refer to this study by its identifier: NCT02021487

University Hospital
Strasbourg, France, 67000
Sponsors and Collaborators
University Hospital, Strasbourg, France
Principal Investigator: Patrick OHLMANN, MD University Hospital, Strasbourg, France
  More Information

Responsible Party: University Hospital, Strasbourg, France Identifier: NCT02021487     History of Changes
Other Study ID Numbers: 5515 
Study First Received: December 19, 2013
Last Updated: December 19, 2013

Additional relevant MeSH terms:
Myocardial Infarction
Pathologic Processes
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases processed this record on January 23, 2017