About this trial
This study aims to evaluate patients undergoing coronary angiography by comparing the use of Potassium Ferrate Hemostatic Sealant (PFHS) in addition to the standard of care (SOC) pneumatic radial compression device versus SOC alone. The objective is to determine whether the addition of PFHS reduces the time to successful deflation and removal of the radial compression device.
Eligibility criteria
Qualifiers
Age ≥ 18 years • Undergoing trans radial coronary angiography with or without PCI
Radial 6Fr Prelude sheath used for the procedure
Planned use of Inflation band (Sunny Medical) radial compression device for hemostasis
Able to provide informed consent
Disqualifiers
On a GPIIB/IIIA inhibitor
Known hypersensitivity to device materials
Infection or serious skin disease at puncture site
Abnormal collateral circulation test / insufficient dual arterial supply
Trial design
Treatments tested in this trial
- Experimental: PFHS + pneumatic radial compression device
- Pneumatic radial compression device alone.