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The Safe and Fast Radial Hemostasis using Synergistic Strategies (SAFE & FAST) trial is an interventional study aimed at reducing the incidence of radial artery occlusion (RAO) rebound bleeding, and the required compression time after transradial approach (TRA) procedures, which have become the default access for coronary procedures globally. The hypothesis is that combining lower-dose heparin and radial hemostasis with simultaneous ipsilateral ulnar artery compression could achieve these improved outcomes.
Patients referred for diagnostic trans-radial cardiac catheterization who meet the inclusion criteria will be randomized into two groups. Group 1 will receive a standard heparin dose (50 U/Kg) with a total compression time of 2 hours using the TR band ® . Group 2 will receive a reduced heparin dose (25 U/Kg) and a compression time of 60 minutes using the VASOBand™, with simultaneous ipsilateral ulnar artery compression.
The study's primary endpoint is a composite of rebound bleeding, post-procedural RAO, and hematoma formation. Radial artery patency will be evaluated using ultrasonography.
With an expected complication rate of 8.2% in Group 1 and 4.5% in Group 2, a sample size of 207 patients per group will provide an 80% power to demonstrate non-inferiority for the treatment group at the alpha 2.5% level. The statistical analysis plan will use descriptive statistics for baseline data and 95% confidence intervals for outcome variables. If non-inferiority is demonstrated, there will be a superiority test performed to examine if Group 2 is superior.
In conclusion, the SAFE & FAST trial intends to establish a safer, quicker protocol for hemostasis after TRA procedures, with the potential to reduce patient recovery time and improve procedure throughput in cardiac catheterization laboratories.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group 1-Regular dose heparin | Active Comparator | Patients in this arm will be labeled as Group 1. Patients will receive a standard heparin dose (50U/Kg) with a total compression time of 2 hours using the TR band ®. |
|
| Group 2-Low dose heparin | Experimental | Patients in this arm will be labeled as Group 2. Patients will receive a reduced heparin dose (25 U/Kg) and a compression time of 60 minutes using the VASOBandâ„¢, with simultaneous ipsilateral ulnar artery compression. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Heparin | Drug | The intervention for this study is the dose of heparin. Patients randomized to group 1 will receive a heparin dose of 50U/kg and those in group 2 will receive a lower dose of heparin at 25U/kg. Recovery period for group 1 would be 2 hours whereas for group 2 would be 1 hour. |
| Measure | Description | Time Frame |
|---|---|---|
| Rebound bleeding | Rebound bleeding necessitating the reapplication of the hemostatic compression. | 24 hours |
| Radial artery occlusion | Post-procedural predischarge radial artery occlusion is evaluated between 30 minutes and 24 hours after the procedure. | 24 hours |
| Hematoma formation | Hematoma formation during or after the procedure as ranked by the EASY criteria. | 24 hours |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Nishant Sethi, MD | Regional Hospital of Scranton | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Regional Hospital of Scranton | Scranton | Pennsylvania | 18510 | United States | ||
| Apex Heart Institute |
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| Label | URL |
|---|---|
| Radial Artery Occlusion After Transradial Interventions: A Systematic Review and Meta-Analysis | View source |
| Influence of the ratio between radial artery inner diameter and sheath outer diameter on radial artery flow after transradial coronary intervention | View source |
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| ID | Term |
|---|---|
| D002318 | Cardiovascular Diseases |
| D006470 | Hemorrhage |
| D001157 | Arterial Occlusive Diseases |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D014652 | Vascular Diseases |
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| ID | Term |
|---|---|
| D006493 | Heparin |
| ID | Term |
|---|---|
| D006025 | Glycosaminoglycans |
| D011134 | Polysaccharides |
| D002241 | Carbohydrates |
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Randomized Controlled Trial
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|
| Terumo Radial Band | Device | Group 1 will receive TR band post cardiac catheterization for radial hemostasis. |
|
|
| Vaosband | Device | Group 2 will receive Vasoband post cardiac catheterization for radial hemostasis. |
|
| Ahmedabad |
| Gujarat |
| 380059 |
| India |
| Multicenter Randomized Evaluation of High Versus Standard Heparin Dose on Incident Radial Arterial Occlusion After Transradial Coronary Angiography: The SPIRIT OF ARTEMIS Study | View source |
| Randomized clinical trial on short-time compression with Kaolin-filled pad: a new strategy to avoid early bleeding and subacute radial artery occlusion after percutaneous coronary intervention | View source |
| The Leipzig prospective vascular ultrasound registry in radial artery catheterization: impact of sheath size on vascular complications | View source |
| Incidence, predictors, and clinical impact of bleeding after transradial coronary stenting and maximal antiplatelet therapy | View source |
| Randomized COmparison of Isolated Radial Artery ComPrEssioN Versus Radial and Ipsilateral Ulnar Artery Compression in Achieving Radial Artery Patency: The OPEN-Radial Trial | View source |