NCT07482865Recruiting
Routine Versus Provisional Distal Perfusion Catheter Placement in Patients Undergoing Mechanical Circulatory Support
Source: ClinicalTrials.gov · Last updated 23 Oct 2026
Brief summary (registry, in English)
A prospective, multi-center, open label, randomized controlled, superiority trial to compare clinical outcomes between routine distal perfusion catheter (DPC) insertion versus provisional distal perfusion catheter (DPC) insertion in the occurrence of sign or symptom of acute limb ischemia in patients undergoing mechanical circulatory support (MCS) through femoral artery approach.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 500 (estimated)
- First submitted
- 15 Mar 2026
- Start date
- 8 Jul 2026
- Primary completion date
- 31 Aug 2030
- Lead sponsor
- Samsung Medical Center
- Diseases
- Heart failure, Coronary artery disease
- NCT number
- NCT07482865
What you commit to
- Study type: Interventional
- Planned participants: 500
- From 8 Jul 2026 to the primary completion date, 31 Aug 2030
- 6 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Irreversible limb ischemia requiring interventional procedures or surgery at the time of MCS insertion
- Previous history if femoral-femoral bypass grafting or femoral-popliteal bypass grafting
- Previous history of limb amputation
Other illness
- Significant coagulopathy precluding invasive procedure due to high risk of bleeding
Other
- Apparent symptoms and sign of acute limb ischemia immediately after mechanical circulatory support insertion
- Pregnant women, women with potential childbearing, or lactating women
- Unwilling or unable to obtain informed consent from the participant or legally authorized representative
Who the study is looking for
- Patients aged 19 years old
- Cardiogenic shock requiring mechanical circulatory support through femoral artery approach
- Subject who can verbally confirm understandings of risks and benefits of receiving distal perfusion catheter insertion and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
- Under the critically-ill clinical circumstance (unclear consciousness of patient), legally authorized representative can provide written informed consent prior to any study related procedure.
Age in the registry: 19 years to - · Sex: All · Does not accept healthy volunteers
Sites (6)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Gyeongsang National University Changwon hospital Coordinator of this site? Confirm its status | Changwon | South Korea | Not yet recruiting |
| Samsung Medical Center Changwon Hospital Coordinator of this site? Confirm its status | Changwon | South Korea | Not yet recruiting |
| Kwandong University Intl. ST. Mary's Hospital Coordinator of this site? Confirm its status | Incheon | South Korea | Not yet recruiting |
| Eunpyeong St. Mary's Hospital Coordinator of this site? Confirm its status | Seoul | South Korea | Not yet recruiting |
| Korea University Anam Hospital Coordinator of this site? Confirm its status | Seoul | South Korea | Not yet recruiting |
| Samsung Medical Center Coordinator of this site? Confirm its status | Seoul | South Korea | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.