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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02591264
Other study ID # 90-14-HYMC
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 28, 2015
Last updated October 28, 2015
Start date November 2015
Est. completion date November 2016

Study information

Verified date October 2015
Source Hillel Yaffe Medical Center
Contact Rami Abu Fanne, MD, PhD
Phone 972-50-3573694
Email ramia@hadassah.org.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

The aim of this study is to determine the role of human neutrophil peptide-1 to 3 in the occurrence of periprocedural myocardial infarction.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 120
Est. completion date November 2016
Est. primary completion date November 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Troponin negative patients

- Stable angina

- Unstable angina

- Positive screening tests

Exclusion Criteria:

- Troponin positive

- Technical failure of procedure

- Hemodynamic unstability

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Blood sample
Blood sample drawn from participants for analysis of neutrophil peptide level

Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Human Neutrophil Peptide Level Laboratory analysis and measurement of Human Neutrophil Peptide-1 to 3 levels Two hours No
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