Aurora Health Care
Milwaukee, Wisconsin, 53202, United States
NCT Number: NCT03522077
The primary objective of this study is to determine if there is a reduction in time to hemostasis in subjects treated with SoftSeal®-STF hemostatic pad when used in conjunction with a vascular compression device after radial transcatheter procedure.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Milwaukee, Wisconsin, 53202, United States
The SoftSeal-STF hemostatic pad and compression devices (TR BAND® and RadAR EasyCLik) function to stop bleeding without obstructing radial artery flow, and have been shown to reduce the occurrence of radial artery occlusion.
The SoftSeal-STF hemostatic pad is an FDA-approved, chitosan-based, non-woven pad with a unique, proprietary fiber structure that when hydrated with tissue fluids forms a gel-like synthetic clot. Its mechanism of action is believed to be due to bioadhesion between the chitosan polymer chains, which are positively charged, and the negatively charged blood and tissue components, thereby stopping bleeding.
In this study the RadAR EasyCLik and TR BAND® Compression devices will be used with the SoftSeal®-STF hemostatic pad to promote hemostasis at the puncture site. Both vascular compression devices are FDA approved.
The VascBand™ Hemostat is an FDA-approved compression device designed to assist hemostasis of arterial, venous and hemodialysis percutaneous access sites.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Chitosan-based, non-woven pad with a unique, proprietary fiber structure that when hydrated with tissue fluids forms a gel-like synthetic clot in conjunction with the RadAR EasyCLik compression device
Chitosan-based, non-woven pad with a unique, proprietary fiber structure that when hydrated with tissue fluids forms a gel-like synthetic clot in conjunction with the TR BAND® compression device
Chitosan-based, non-woven pad with a unique, proprietary fiber structure that when hydrated with tissue fluids forms a gel-like synthetic clot
The VascBand™ Hemostat is an FDA-approved compression device designed to assist hemostasis of arterial, venous and hemodialysis percutaneous access sites.
Time frame: 1 day
Time interval in minutes beginning with sheath removal and ending with removal of hemostatic device and/or observed hemostasis
Time frame: Post procedure to prior to discharge, on average same day discharge or up to 1-2 days
A ≥ 3 mg/dL drop in hemoglobin, or required blood transfusion or vascular repair to control bleeding. Prior to discharge.
Time frame: Post procedure to prior to discharge, on average same day discharge or up to 1-2 days
Number of participants with light access site bleeding without hematoma formation
Time frame: At time of follow up office visit, if done within 45 days post procedure
Number of participants with light access site bleeding without hematoma formation
Time frame: 1 day
Number of participants with hematoma formation ≥ 3 cm in diameter
Time frame: 3 day
Pain at access site on numeric scale of 0-10, 0 meaning no pain at all and 10 meaning extreme pain. A lower score is a better outcome and higher score is a worse outcome.
Time frame: At time of follow up office visit, if done within 45 days post procedure
Pain at access site on numeric scale of 0-10, 0 meaning no pain at all and 10 meaning extreme pain. A lower score is a better outcome and higher score is a worse outcome.
Time frame: 3 days
Reported as pain, tingling, or numbness in the hand and/or fingers reported
Time frame: 30 days
Reported as pain, tingling, or numbness in the hand and/or fingers reported
Time frame: 30 days
Number of Participants who had a Readmission for a Vascular complication
Time frame: 30 days
Number of participants with bruising, swelling, or redness at or near access site
Time frame: At time of follow up office visit, if done within 45 days post procedure
Reported as average, above average, or excellent satisfaction with procedure
Time frame: At time of follow up office visit, if done within 45 days post procedure
Satisfaction with healing post procedure, reported as average, above average, or excellent
Wake Forest University Health Sciences
Other
RAVE: Radial Artery Vascular Complication and Resource Utilization in Subjects Undergoing an Angiogram/PCI (Percutaneous Coronary Intervention)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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