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Humanin Isoforms in Cardiac Muscle and Blood Plasma and Major Complications After Cardiac Operation

Prospective Clinical Observational Study of Humanin Isoforms in Cardiac Muscle and Blood Plasma and Their Association to Major Complications After Cardiac Operation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03431844
Enrollment
106
Registered
2018-02-13
Start date
2018-01-01
Completion date
2019-08-31
Last updated
2020-08-05

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

Conditions

Coronary Artery Bypass Surgery, Myocardial Ischemia

Brief summary

Objective of the study is to clarify humanin-like peptide concentration in myocard tissue and in blood and to study if its concentration level is related to early complication occurrence and frequency after cardiac operation. Hypothesis of the study is that previously described elements are related to each other.

Detailed description

Data collection: Historical medical and preoperative data, operation data (type of operation performed and its details), detailed postoperative course (occurrence of complications). Specimen collection: * Tissue sample is taken during the operation from the right atrial appendage of the heart and the sample is frozen at -80 C. * Blood samples are taken just before the operation, one hour after aortic cross-clamp removal and the next morning after the operation. Samples are processed and blood plasma is frozen at -80 C.

Interventions

None listed

Sponsors

Tartu University Hospital
CollaboratorOTHER
North Estonia Medical Centre
CollaboratorOTHER
University of Tartu
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age at least 18 years * Ischemic heart disease in medical history * Planned on-pump coronary artery bypass graft (CABG) operation * Signed informed consent by patient

Exclusion criteria

* Age \<18 years * Planned isolate valve or aortic operation * Patient is in another study with an intervention * Absence of signed informed consent

Design outcomes

Primary

MeasureTime frameDescription
Mortality30 days30-day all-cause mortality
Major complications: myocardial infarction.30 daysDiagnosed myocardial infarction.
Major complications: acute kidney injury.30 daysDiagnosed acute kidney failure (KDIGO stage).
Major complications: stroke.30 daysDiagnosed stroke.

Countries

Estonia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026