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RecruitingNCT05935397HYUMCUpdated Jul 7, 2023

HanYang University Medical Center (HYUMC) Registry

An observational study in Coronary Artery Stenosis, Coronary Artery Disease and Blood Pressure, sponsored by Hanyang University Seoul Hospital. Recruiting at 3 sites in Korea, Republic of. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2023-07-07.

Sponsored by Hanyang University Seoul Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as recruiting.
  • Started Jan 2012; still recruiting 14 years 10 months later.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
5,000
Ages
19 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 31 studies in Coronary Stenosis with a site in Korea, Republic of — 9 open to participants now, 10 under way, none of them phase 3. Coronary Stenosis · Korea, Republic of.

Planned enrollment
Largest of 16
5,000 · median 1,000
Started
2012
the only one that year
Observational
16 of 31
6 open now
Registered
26th of 31
by date

Among the 31 studies in Coronary Stenosis with a site in Korea, Republic of, this one has the largest planned enrollment of the 16 observational ones that give a count, is the only one that started in 2012, is one of 16 observational ones, and was the 26th registered.

Coronary Stenosis

326 studies on the registry are indexed under Coronary Stenosis; 57 are open to participants now.

Browse Coronary Stenosis studies →

Open to participants now

9 of the 31 studies in Coronary Stenosis with a site in Korea, Republic of are open now. Recruiting first, the newest first:

3 more — sign in →

All 9 open studies →

A study can be open while its sites in Korea, Republic of have not opened yet or have stopped. Only those recruiting at a site in Korea, Republic of →

Who these studies take

Of the 40 Coronary Stenosis studies recruiting now, 33 (83%) set no upper age limit and 3 (8%) stop at 75 or younger; 4 take children under 18; 2 take healthy volunteers.

This study: 19 Years and older · all sexes · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 31 studies in Coronary Stenosis with a site in Korea, Republic of, or all of them as a file.
02

Study summary

The HYUMC registry is a two-center, real-world registry of percutaneous coronary intervention in patients with coronary artery disease. From January 2012, PCI-treated patients from Hanyang University Seoul Hospitals and Hanyang University Guri Hospitals were enrolled in this registry.

The aim of this registry is to examine the long-term clinical outcomes and identify predictors of adverse outcomes following percutaneous coronary intervention conducted at academic hospitals.

Read the detailed description

In the HYUMC registry, the researchers have gathered and assessed various demographic, laboratory, echocardiographic, and angiographic measurements (both on-admission and during follow-up), as well as conducted questionnaires among patients who underwent percutaneous coronary intervention. The primary focus of this registry is to examine the effects of these parameters on long-term clinical outcomes.

03

Conditions studied

  • Coronary Artery Stenosis
  • Coronary Artery Disease
  • Blood Pressure
04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Consecutive patients with CAD

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Consecutive patients with CAD who underwent PCI one or more drug eluting stent (DES) with from 2012 at the Division of Cardiology of Hanyang University Seoul Hospital and Hanyang University Guri Hospital, Korea.

Exclusion criteria

Exclusion Criteria:

  • second or subsequent hospitalization records of patients with multiple admissions
  • patients who died during index hospitalization
  • patients who treated with first-generation drug eluting stent
  • patients with an outpatient follow-up record of less than 6 months
  • patients with insufficient medical records.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
5,000 participants (estimated)
Target follow-up
10 Years
Patient registry
Yes

Groups and cohorts

  • patients with CAD undergoing PCI

    patients with CAD undergoing PCI with second generation DES

    Device: percutaneous coronary intervention

Interventions

  • Devicepercutaneous coronary intervention

    patients with CAD undergoing PCI with second generation DES

06

What researchers measure

Primary outcomes

  1. MACCE (major adverse cardiac and cerebrovascular event)

    the composite of all-cause death, myocardial infarction, stroke, or any revascularization

    Time frame: 10-year

Secondary outcomes

  1. All-cause death

    death from any cause

    Time frame: 10-year

  2. Myocardial infarction,

    presence of clinical symptoms with the presence of electrocardiographic changes, or imaging evidence of new loss of viable myocardium or new regional wall motion abnormalities, in conjunction with elevated levels of cardiac biomarker above the 99th percentile upper reference limit

    Time frame: 10-year

  3. Stroke

    neurological deficit resulting from acute focal damage to the central nervous system due to a vascular cause, requiring hospitalization, and confirmed by a neurologist through imaging findings

    Time frame: 10-year

  4. Any revascularization

    PCI or coronary artery bypass surgery on either target or nontarget vessels

    Time frame: 10-year

07

Study locations

3 of 3 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided — The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2012 (actual). Primary completion is estimated for Dec 2025, 167 months after the start.

Of 58 observational studies under Coronary Stenosis, half reached primary completion within 29 months of starting (the median), counting those still running; a quarter within 15 and three quarters within 143. This study's planned 167 months is above that.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 29, 2023
First posted
Jul 7, 2023
StartActual
Jan 1, 2012
Primary completionEst.
Dec 31, 2025
CompletionEst.
Dec 31, 2025
Last update
Jul 7, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 7, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05935397
Lead sponsor
Hanyang University Seoul Hospital
Collaborators
Hanyang University
Responsible party
Young-Hyo Lim (Prof., Hanyang University Seoul Hospital) — Principal investigator
First posted
Jul 7, 2023
Start date
Jan 1, 2012
Primary completion
Dec 31, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Jul 7, 2023

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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