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Prospective angioscopic Observation of vascular wall Re-intimal Coverage over DES IN the Infra-inguinal lesion

Prospective angioscopic Observation of vascular wall Re-intimal Coverage over DES IN the Infra-inguinal lesion - PORCINII trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000018862
Enrollment
50
Registered
2015-08-31
Start date
2013-10-01
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

Peripheral Arterial Disease

Interventions

None listed

Sponsors

Kansai Rosai Hospital
Lead Sponsor
Kobe University, Saiseikai Nakatsu Hospital, Hyogo college of medicine, Omihachiman Community Medical Center, Kyoto university
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) PAD patients undergoing DES(Zilver PTX) inplantation at SFA or PA 2) DES inplantation site can be applyed angioscopic analyse. 3) Patients who can take both of aspirin and clopidogrel. 4) Patients who have provided informed consent written by themselves.

Exclusion criteria

Exclusion criteria: 1) Patients who had prior stenting, or subject limb need DES and BMS at once. 2) Paients who need other blood thinner besides aspirin and clopidogrel. 3) Patients who participate in clinical trials(besides PhIV). 4) Female patient during pregnancyor breast-feeding. 5) Patients who need hemodialysis. 6) Patients judged as unsuitable for the study by the investigator for other reasons.

Design outcomes

Primary

MeasureTime frame
Neoitimal coverage and intra-stent thrombi by angioscopic analysis.

Countries

Japan

Contacts

Public ContactOsamu Iida

Kansai Rosai Hospital Cardiovascular Medicine

iida.osa@gmail.com06-6416-1221

Outcome results

None listed

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