Measuring Blood Flow in Heart Vessels With a New Fibre Optic Sensor

NACompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

December 14, 2022

Primary Completion Date

August 22, 2023

Study Completion Date

October 3, 2023

Conditions
Coronary Artery DiseaseCoronary StenosisCoronary Microvascular Disease
Interventions
DEVICE

Intra coronary rapid-exchange iKOs microcatheter intervention

Patients planned for an invasive coronary physiology (pressure-wire) study and who meet the inclusion criteria and none of the exclusion criteria can be enrolled. Participants will undergo preparation for their clinical procedure (angiogram with pressure wire study) in the normal manner. Arterial cannulation will be performed via the radial or femoral artery) under local anaesthesia. The sheath will be inserted and a pre-procedure blood sample taken for Troponin T level. A coronary angiogram will be performed as per standard clinical practice prior to cannulating the coronary artery to be studied. The pressure studies will be performed sequentially, first with a pressure wire before using the iKOs™ microcatheter. Following withdrawal of the iKOs™ microcatheter. A pressure wire assessment is repeated after the microcatheter is withdrawn. The case will then proceed as clinically indicated. Post-procedure the participant will be managed according to standard clinical practice.

Trial Locations (1)

EC1A 7BE

St Bartholomew's Hospital, London

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Echopoint Medical Ltd

UNKNOWN

lead

Queen Mary University of London

OTHER