Percutaneous Coronary Intervention (PCI) Clinical Trials

Clinical trials related to Percutaneous Coronary Intervention (PCI) Procedure

Comparative Evaluation of Sustained meChanical AsPiration Thrombectomy and no Thrombus Modification for Pre-stent Thrombus bUrden Reduction in Patients With Acute Myocardial Infarction Study: the CAPTURE AMI Study

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Device
Study Type: Interventional
Study Phase: Phase 2/Phase 3
SUMMARY

The CAPTURE AMI trial is an investigator-initiated, single-centre, two-arm, randomised controlled trial. Patients aged ≥ 18 years who present with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (pPCI) will be enrolled after angiographic evidence of a high thrombus burden (TIMI thrombus grade ≥ 4) and meeting the inclusion criteria laid out in section 9.2 will be 1:1 randomised to receive either standalone PCI (Arm 1) or adjunct sustained mechanical thrombectomy + PCI (Arm 2). The CAPTURE AMI study will enrol specifically patients with: A. Evidence of high thrombus burden on coronary angiography (TIMI thrombus grade ≥ 4) B. Culprit in an artery with a diameter of 3.0 mm or more. The trial is designed to evaluate the efficacy of sustained mechanical thrombectomy versus standalone PCI in patients with a large thrombus burden assessed angiographically, with a pre-stent thrombus burden (%) as the primary imaging endpoint.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Primary PCI patient with ST elevation myocardial infarction

• Angiographic criteria:

‣ TIMI 0/1 flow at presentation

⁃ Angiographic thrombus score ≥ 4

⁃ Vessel diameter at site of occlusion ≥ 3.0mm (determined by coronary angiography)

Locations
Other Locations
United Kingdom
Oxford Heart Centre - John Radcliffe Hospital
RECRUITING
Oxford
Contact Information
Primary
Giovanni Luigi De Maria, MD
GiovanniLuigi.DeMaria@ouh.nhs.uk
+44 18655 528364
Time Frame
Start Date: 2026-07-08
Estimated Completion Date: 2028-01-08
Participants
Target number of participants: 60
Treatments
Active_comparator: Standalone PCI
Standalone OCT guided PCI
Experimental: PCI & Sustained thrombectomy
OCT guided PCI \& Sustained Thrombectomy
Sponsors
Leads: Oxford University Hospitals NHS Trust

This content was sourced from clinicaltrials.gov