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Outcome in Hemodialysis of Promus stent

Outcome in Hemodialysis of Promus stent - OUCH-PRO

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006684
Enrollment
120
Registered
2011-11-08
Start date
2011-11-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Ischemic heart disease Chronic renal failure on hemodialysis

Interventions

PCI with Promus stent

Sponsors

Coronary Intervention Trial and Evaluation group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patints with chronic renal failure on hemodialysis Elective PCI for Ischemic heart disease using Promus stent

Exclusion criteria

Exclusion criteria: CPA Cardiogenic shock Emergent PCI STEMI Intolerance with antiplatelet therapy Planned PCI for other lesions in 6 months Restenosis after DES Severe valvular heart disease Critical limb ischemia CTO No indication for PCI

Design outcomes

Primary

MeasureTime frame
Target Vessel Failure including cardiac death, myocardial infarction in the target vessel and target vessel revascularization at 12 months

Secondary

MeasureTime frame
Binary restenosis rate by QCA Late lumen loss by QCA Death, TLR, MACE at 12 months Stent thrombosis rate Neointimal volume by IVUS osteoprotegerin and MACE rate Dialyzer and MACE rate or late lumen loss

Countries

Japan

Contacts

Public ContactSachiko Yajima

Tokai University Cardiovascular Medicine

s.yajima@tokai-u.jp0463-93-1121

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026