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Gyeongsang National University Hospital Registry

G-NUH (Gyeongsang National University Hospital) Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04650529
Acronym
GNUH
Enrollment
10000
Registered
2020-12-02
Start date
2010-01-31
Completion date
2025-12-31
Last updated
2021-01-27

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

Conditions

Blood Clot, Hemostatic Disorder, Percutaneous Coronary Intervention

Keywords

East Asian Paradox

Brief summary

The G-NUH registry is a two-center, real-world registry of percutaneous coronary intervention in patients with significant coronary artery disease. From January 2010, PCI-treated patients from Gyeonsang National University Hospitals (Jinju & Changwon) were enrolled in this registry. The aim of this registry is to investigate long-term clinical outcomes and predictors of adverse outcomes after percutaneous coronary intervention from the academic hospitals.

Detailed description

In the G-NUH registry, the investigators have collected and measured multiple hemostatic, physiologic and laboratory measurements (on-admission & 1-month) and questionnarred from PCI-treated patients. This registry will focus on the impacts of these parameters on long-term clinical outcomes from East Asian patients.

Interventions

DEVICEstent, ballooning

DES, BMS, BRS, DEB, and POBA can be used for PCI

Sponsors

Gyeongsang National University Hospital
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 \>= 18 years * Significant coronary artery disease * Treated with PCI * Multiple hemostatic or physiologic measurements

Exclusion criteria

* Medically treated cases

Design outcomes

Primary

MeasureTime frameDescription
MACEup to 10 yearsthe composite of cardiovascular death, myocardial infarction or stroke

Secondary

MeasureTime frameDescription
Revascularizationup to 10 yearstarget-lesion, target-vessel vs. nontarget-vessel
Major bleedingup to 10 yearsBARC type 3-5
Stent thrombosisup to 10 yearsThrombotic events in & near to stent
ISRup to 10 yearsin-stent restenosis
Strokeup to 10 yearsIschemic & hemorrhagic stroke
Myocardial infarctionup to 10 yearsFatal & non-fatal myocardial infarction
Cardiovascular deathup to 10 yearsMortality related with cardiovascular events

Other

MeasureTime frameDescription
Incidence of MACE according to cardiac contractilityup to 10 yearsEchocardiography: LV EF, E/A, TR Vmax, LAVI
Incidence of MACE according to physiologic indexup to 10 yearsfractional flow reserve (FFR), coronary flow reserve (CFR) and the index of microvascular resistance (IMR)
Incidence of MACE according to 1-month bleeding & dyspnea episodesup to 10 yearsQestionnarres for bleeding, dyspnea, side effects
Incidence of MACE according to platelet functionup to 10 yearsVerifyNow assay
Incidence of MACE according to global hemostasis assayup to 10 yearsthromboelastography (TEG: R, alpha angle, MA and LY30)
Incidence of MACE according to hemostatic biomarkersup to 10 yearshs-CRP, fibrinogen, D-dimer, NT-proBNP, lipid battery

Countries

South Korea

Contacts

Primary ContactJin Sin Koh, MD, PhD
kjs0175@gmail.com82-10-8544-0175

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026