Clinical trials: Hemostasis Compression Device
Atrial Fibrillation, Hemostasis
Vascular Closure With a Device Compared to Manual Compression After Atrial Fibrillation Ablation: The LockeT II Study
The LockeT II study is a single center, prospective randomized study. It is intended to study the effectiveness of using LockeT device to gain hemostasis after venous procedures as compared to Manual Compression (MC).
- Trial name
- NCT06078735
- Testing
- Vascular closure with LockeT device
- Where
- 6 sites in United States
- Volunteers
- 110 people
- Sponsor
- Kansas City Heart Rhythm Research Foundation
Atrial Fibrillation, Hemostasis
Vascular Closure With Novel External Compression Device: The LockeT Study
Single center, retrospective review study comparing Figure of Eight suture to LockeT, enrolling approximately 70 patients.
- Trial name
- NCT06199414
- Testing
- Venous Closure
- Where
- 2 sites in United States
- Volunteers
- 70 people
- Sponsor
- Kansas City Heart Rhythm Research Foundation
Brachial Access, Access Complication
Evaluation of Shoulder Access Safety Using the NewMan Compression Device
The aim of the study is to evaluate the effectiveness of the NewMan compression device in shoulder access in patients with occlusive lesions of the femoral-popliteal segment of the lower extremity arteries by comparing the…
- Conditions
- Brachial Access, Access Complication, Hemostasis Compression Device, Atherosclerosis of the Arteries of the Lower Extremities
- Trial name
- SAND (NCT07714824)
- Testing
- Hemostasis is performed using a pressure bandage, Hemostasis is performed using the NewMan compression device
- Where
- Russia
- Volunteers
- 229 people
- Sponsor
- Pirogov Russian National Research Medical University
Peripheral Artery Occlusion, Hemostasis
Comparison Study of Compression Devices Used in Transradial Coronary Angiography
The transradial route is used in 90% of the coronary angiograms performed at Oslo University Hospital (OUS), Ullevål. A compression device needs to be applied after the procedure to achieve hemostasis.
- Conditions
- Peripheral Artery Occlusion, Hemostasis, Injury of Radial Artery
- Trial name
- NCT02583854
- Testing
- RY-STOP hemostasis device, TR-Band, Terumo
- Where
- Norway
- Volunteers
- 499 people, healthy volunteers welcome
- Sponsor
- Oslo University Hospital
Common Femoral Artery Injury, Other Vascular Adverse Event
Efficacy Study of Assiut Femoral Compression Device Versus Manual Compression in the Achievement of Hemostasis
This study was performed to evaluate the safety and efficacy of a locally designed Assiut Femoral Compression Device (AFCD) versus manual compression (MC).
- Trial name
- NCT02214030
- Testing
- Assiut Femoral Compression Device
- Where
- Egypt
- Sponsor
- Assiut University
Post Dialysis Arterio-Venous Fistula Puncture Sites
Applying Moziak Device Compared to Standard Manual Compression on Arterio-Venous Fistula Puncture Sites Haemostasis
The study aimed to evaluate the Effectiveness of Applying Moziak Device Compared to Standard Manual Compression Post Dialysis Arterio-Venous Fistula Puncture Sites Haemostasis
- Trial name
- NCT05463315
- Testing
- Moziak Device
- Where
- Egypt
- Volunteers
- 96 people
- Sponsor
- Beni-Suef University
Coronary Artery Disease
The Study for Evaluate of Satety and Dfficacy of Hemostatic Device
The goal of this clinical trial is to compare the new pneumatic compression device TRAcelet with conventional compression method in patients undergone transradial coronary angiography.
- Trial name
- NCT06590571
- Testing
- TRAcelet™, Gauze pad
- Where
- South Korea
- Volunteers
- 227 people, healthy volunteers welcome
- Sponsor
- Pusan National University Yangsan Hospital
Coronary Artery Disease With Myocardial Infarction
Comparison of 2 Hemostasis Techniques After Transradial Coronary
Randomized clinical trial to compare radial artery patency after transradial coronary catheterization using 2 different hemostasis techniques.
- Trial name
- NCT02873871
- Testing
- Standardized compressive dressing, Hemostasis with TerumoBand®
- Where
- Brazil
- Volunteers
- 600 people
- Sponsor
- Hospital de Clinicas de Porto Alegre
Radial Artery Occlusion, Cardiac Catheterization
Manual vs Pneumatic Compression to Prevent Radial Artery Occlusion After Transradial Procedures
This study evaluates two commonly used methods of achieving hemostasis after transradial cardiac catheterization: manual compression and pneumatic compression with gradual deflation.
- Trial name
- RADIAL-HEMO (NCT07621185)
- Testing
- Manual Radial Compression, Pneumatic Radial Compression Device
- Where
- Spain
- Volunteers
- 1,168 people
- Sponsor
- Hospital Clinic of Barcelona
Coronary Angioplasty, Coronary Artery Disease
Arterial Closure vs Direct Compression for Hemostasis After PCI - The ACDC Trial
Hemostasis at the arterial puncture site after percutaneous coronary interventions is achieved by either placement of a puncture closure device or by delaying sheath removal for hours to allow normalization of heparin induced…
- Trial name
- NCT00264264
- Testing
- Closure Device, Direct Compression
- Where
- Canada
- Volunteers
- 572 people
- Sponsor
- Unity Health Toronto
Peripheral Vascular Disease, Coronary Artery Disease
Angio-Seal Evolution Device Registry
Collect data on the use of the Angio-Seal Evolution Device in diagnostic and interventional patient populations.
- Conditions
- Peripheral Vascular Disease, Coronary Artery Disease, Peripheral Artery Disease, Arterial Occlusive Disease
- Trial name
- NCT00817349
- Where
- 10 sites in United States
- Volunteers
- 1,004 people
- Sponsor
- Abbott Medical Devices
Sealing the Arteriotomy
Evaluation of the CloSys Closure System as an Adjunct to Standard Compression
The purpose of this study is to evaluate the safety and efficacy of the CloSys Hemostatic Device designed to stop bleeding after an interventional procedure.
- Trial name
- NCT00963690
- Testing
- CloSys Hemostatic Device (HD), Standard compression
- Where
- 2 sites in United States
- Volunteers
- 30 people
- Sponsor
- CloSys Corporation