Hemostasis Clinical Trial
Official title:
ACCEL® Absorbable Hemostat Powder Clinical Trial
The ACCEL® Absorbable Hemostat Powder Clinical IDE Trial is designed as a prospective, multi-center, randomized, non-inferiority, controlled pivotal clinical trial to evaluate the safety and efficacy of the ACCEL® Absorbable Hemostat Powder as compared to gelatin sponge, for achieving hemostasis in subjects undergoing cardiovascular, liver, or soft tissue surgery, when control of oozing to moderate bleeding by standard surgical techniques is ineffective and/or impractical.
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05335525 -
Post-market Clinical Investigation of the Angio-Seal™ VIP VCD (ANGIO-SEAL CLOSE)
|
||
| Completed |
NCT02583854 -
Comparison Study of Compression Devices Used in Transradial Coronary Angiography
|
N/A | |
| Recruiting |
NCT05977946 -
Delivering Transcutaneous Auricular Neurostimulation to Regulate Platelet Activity in Healthy Human Subjects
|
N/A | |
| Completed |
NCT01388491 -
A Multinational Study to Evaluate the Effects of a 28-Day Oral Contraceptive on Hemostatic Parameters in Healthy Women
|
Phase 2 | |
| Recruiting |
NCT05323448 -
Efficacy of ARISTA-AH for Restoring Hemostasis Following Posterior Long-segment Spinal Fusion.
|
N/A | |
| Recruiting |
NCT06078735 -
Vascular Closure With a Device Compared to Manual Compression After Atrial Fibrillation Ablation: The LockeT II Study
|
N/A | |
| Completed |
NCT03907111 -
Compare the Hemostatic Effectiveness of Chitosan Gauze With Traditional Gauze on Open Wound on 10 Participants.
|
N/A | |
| Recruiting |
NCT05875272 -
Interchangeability of Arterial Coagulation and Venous Coagulation, in the Context of Cardiac Surgeries Under Cardiopulmonary Bypass, Using the DMDiv Hemochron Signature Elite
|
||
| Completed |
NCT04593667 -
Randomized Study of Accelerated Radial Arterial Hemostasis
|
N/A | |
| Completed |
NCT01252186 -
A Multicenter Study to Evaluate the Effects of a 91-Day Extended Cycle Oral Contraceptive on Hemostatic Parameters in Healthy Women
|
Phase 2 | |
| Terminated |
NCT00802633 -
Radical Cystectomy: Can We Improve Our Surgical Technique With the Ligasure Impact Tissue-Sealing Device?
|
N/A | |
| Completed |
NCT02034799 -
Phase IV Bioseal Study in Brain Tumor Surgery
|
Phase 4 | |
| Terminated |
NCT03873168 -
Post-Market Evaluation of HEMOBLAST™ Bellows in Open Gynecological, Urological, ENT, Head, Neck, and Vascular Surgeries
|
||
| Recruiting |
NCT04377490 -
Thrombo Embolic Events in Hospitalized Patients With Covid-19 Serious Acute Pneumopathy
|
||
| Completed |
NCT00449410 -
Silent Cerebrovascular Lesion and Cognitive Decline Prevention by Cholesterol Lowering in Elderly AF Patients
|
Phase 4 | |
| Completed |
NCT03873181 -
Post-Market Evaluation of HEMOBLAST™ Bellows in Laparoscopic Abdominal, Gynecological, and Urological Surgery
|
||
| Completed |
NCT04660721 -
A Study Evaluating the Safety and Preliminary Efficacy of sFilm-FS in Controlling Parenchymal Bleeding During Elective Hepatic Surgery
|
Phase 1/Phase 2 | |
| Recruiting |
NCT05653843 -
MANTIS Endoscopic Clipping Study
|
||
| Completed |
NCT00658723 -
The Fibrin Patch Soft Tissue Study
|
Phase 2 | |
| Recruiting |
NCT03323359 -
Efficacy and Tolerability of Hemopatch After Hepatic Resection
|
N/A |