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Arginase in Myocardial Infarction

Arginase in Myocardial Infarction - Arginase in Myocardial Infarction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON41863
Enrollment
30
Registered
2015-10-23
Start date
2017-06-27
Completion date
Unknown
Last updated
2024-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Attack Myocardial Infarction

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Individual is * 18 and * 85 years of age 2. Individual has evidence of ST-segment elevated myocardial infarction (ST elevation *2 mm in *2 contiguous leads in V1 through V5) for more than 30 minutes (case) 3. Individual has an anticipated time of symptom onset to reperfusion of *6 hours (case) 4. Individual has an indication for an invasive coronary angiogram. 5. Individual agrees and is competent and willing to provide written, informed consent to participate in this clinical study.

Exclusion criteria

Exclusion criteria: 1. Individual has signs and symptoms of septic shock 2. Individual has a history of urea cycle disorders in wich arginase deficiency is a key factor 3. Individual has a arginine/arginase-dependent malignancy, such as human hepatocellular carcinoma

Design outcomes

Primary

MeasureTime frame
Arginase(ng/ml) will be determined by means of an enzyme-linkend immunosorbent assay (ELISA), its activity will be determined by measurement of arginine-, citruline- and ornithine (arginine metabolite) levels in plasma.

Secondary

MeasureTime frame
none

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)