Safety And Feasibility Study Of Pressure-controlled Intermittent Coronary Sinus Occlusion (PICSO) In Patients With Coronary Artery Disease Undergoing Native Vessel Intervention

PHASE2CompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

October 31, 2010

Primary Completion Date

March 31, 2011

Study Completion Date

April 30, 2011

Conditions
Stable Angina
Interventions
PROCEDURE

PICSO

"* Baseline (hemodynamic) measurement~* Intra coronary~* Blood sampling~* LAD occlusion: for 3 min or until pain with and without PICSO~* Break recovery: the patient can recover from pain for 3 min~* CFIp: by a ComboWire advanced in the center lumen of an occlusion balloon.~* PICSO: start automatically and continued for 10 min.~* PCI/PICSO: concomitantly for the whole duration of the PCI intervention.~* 24h Follow up: additional blood samples every 6 hours (4 times)~* 30 days follow up."

Trial Locations (1)

1105 AZ

Academic Medical Center Amsterdam, Amsterdam

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Miracor Medical SA

INDUSTRY

NCT01308125 - Safety And Feasibility Study Of Pressure-controlled Intermittent Coronary Sinus Occlusion (PICSO) In Patients With Coronary Artery Disease Undergoing Native Vessel Intervention | Biotech Hunter | Biotech Hunter