The Role of Netrin -1 in Acute Coronary Syndrome
ACS-NETRİN-1
The Effect of Serum Netrin-1 Levels on Diagnosis and Prognosis in Patients Presenting to the Emergency Department With Acute Coronary Syndrome
1 other identifier
interventional
238
0 countries
N/A
Brief Summary
In our study, Netrin -1; We found that patients with ACS increased at the time of admission, decreased TIMI 3 flow after angiography, and higher risk groups in high risk groups such as TIMI and GRACE were found to have higher Netrin-1 levels.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2013
Longer than P75 for not_applicable
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
September 15, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 15, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
June 15, 2018
CompletedFirst Submitted
Initial submission to the registry
June 18, 2019
CompletedFirst Posted
Study publicly available on registry
July 19, 2019
CompletedJuly 19, 2019
July 1, 2019
11 months
June 18, 2019
July 18, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
serum netrin-1 value
Netrin-1 in plasma was measured by enzyme-linked immunosorbent assay (ELISA) (Mybıosource MBS044526 ) All assays were performed in duplicate. Plasma Netrin-1 is expressed in picograms (pg) per mg.
30 minute
Study Arms (2)
ACS GRUP
ACTIVE COMPARATORDemographic characteristics, history, vital signs, laboratory findings, coronary angiography (CAG) and echocardiography (ECO) findings of the patients were recorded. Netrin-1 levels were studied with blood collected at the hospital and 6-8 hours after CAG. CAG results were evaluated by TIMI flow. The patients were divided into two groups with and without TIMI 3 flow and Netrin-1 levels were compared. GRACE (Global Registry of Acute Coronary Events) and TIMI (Thrombolysis in Myocardial Ischemia) clinical risk assessments were performed and Netrin-1 values were compared.
plasebo grup
ACTIVE COMPARATORIt consisted of those without any disease and netri-1 values at admission were compared with the uptake patient group.
Interventions
Eligibility Criteria
You may qualify if:
- Patients over the age of 18
- diagnose ACS
- patients undergoing angiography
You may not qualify if:
- CVE history
- Neurological disease
- Pregnancy and Lactation
- Liver failure
- Diagnosed malignity
- Use of anticonvulsant and nephrotoxic medication
- Chronic kidney disease
- Not having angiography
- Developing acute renal failure after angiography
- Patients who rejected to participate were excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Hüseyin Mutlu, MD
Aksaray/Turkey
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Patient group; Those diagnosed with ACS over 18 years of age, planned angiography and accepted angiography. The control group consisted of volunteers without disease.
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst. Prof. Dr. Principal Investigator
Study Record Dates
First Submitted
June 18, 2019
First Posted
July 19, 2019
Study Start
September 15, 2013
Primary Completion
August 15, 2014
Study Completion
June 15, 2018
Last Updated
July 19, 2019
Record last verified: 2019-07
Data Sharing
- IPD Sharing
- Will not share