xDot AMS for Vascular Closure
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new device, the xDot Access Management System (AMS), to ensure its safety and effectiveness in closing large holes in blood vessels, specifically in the upper leg (femoral area) after certain medical procedures. It targets individuals undergoing routine procedures with large instruments in the groin area, such as heart valve repairs or blood vessel treatments. Ideal candidates for this trial are those planning such procedures and having blood vessels in the thigh area that meet specific size and health criteria.
As an unphased trial, participants can contribute to the development of innovative medical solutions.
What prior data suggests that the xDot Access Management System is safe for vascular closure?
Research has shown that the xDot Access Management System (AMS) was safe in earlier studies. Researchers tested it for closing large access points in a major leg artery. These studies aimed to prove the system's safety and effectiveness. The device also received special approval from the FDA for further testing, indicating confidence in its safety.
Although the device remains under study and is not yet for sale, trials have found no major safety problems. While more research is needed, early results suggest it is well-tolerated, with no significant harmful effects reported so far.12345Why are researchers excited about this trial?
Most vascular closure treatments typically rely on manual compression or devices that use collagen plugs to seal vessels. However, the xDot Access Management System (AMS) is unique because it offers a more automated and precise approach to vascular closure. Researchers are excited about this system because it aims to reduce healing time and potential complications by providing a more efficient closure process. This innovative method could significantly improve patient comfort and outcomes by minimizing the risk of bleeding and other complications commonly associated with traditional closure techniques.
What evidence suggests that the xDot Access Management System is effective for vascular closure?
Research has shown that the xDot Access Management System (AMS), which participants in this trial will receive, effectively closes large blood vessel access points. Studies have found that xDot AMS quickly closes these sites, reducing the risk of complications. For example, one study demonstrated that the system can stop bleeding quickly and effectively. Another study confirmed that xDot AMS performs well even in challenging situations, such as when blood vessels are hardened. These findings suggest xDot AMS could be a reliable option for closing blood vessels.12346
Who Is on the Research Team?
Ben Smith, PhD
Principal Investigator
Bright Research, Inc.
Are You a Good Fit for This Trial?
This trial is for adults aged 18–80 who need closure of a large femoral artery or vein after certain procedures. Participants must have suitable blood vessel size and health, be able to give consent, and follow study instructions.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive the xDot Access Management System for closure of large bore femoral-arterial and venous-access sites
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- xDot Access Management System (AMS)
Trial Overview
The study is testing the safety and effectiveness of the xDot Access Management System (AMS), a device used to close large access sites in the femoral artery or vein after medical procedures.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Find a Clinic Near You
Who Is Running the Clinical Trial?
xDot Medical, Inc
Lead Sponsor
Bright Research Partners
Industry Sponsor
Citations
TCT-718 Novel Vascular Closure Device (xDot): Efficacy in ...
This study demonstrates the design robustness and efficacy of the xDot Access Management System for achieving rapid and effective closure in ...
xDot Medical can begin FDA IDE study of vascular closure ...
xDot Medical announced today that it received FDA investigational device exemption (IDE) approval for its access management system (AMS).
xDot Access Management System Early Feasibility Study
The purpose of this study is to demonstrate the safety and assess the effectiveness of the xDot AMS for closing the access sites of the femoral artery (femoral- ...
xDot Access Management System Pivotal Study
The objective of this study is to establish reasonable assurance of safety and effectiveness for the xDot Access Management System (AMS) ...
5.
trial.medpath.com
trial.medpath.com/clinical-trial/4d06e1efd642caae/nct07464353-xdot-access-management-system-closure-large-bore-femoralxDot Access Management System Early... | Clinical Trial
The purpose of this study is to demonstrate the safety and assess the effectiveness of the xDot AMS for closing the access sites of the femoral ...
6.
linkedin.com
linkedin.com/posts/jack-shuang-hou-75314a2b3_receives-ide-approval-activity-7480054258109849600-7p05xDot Medical Receives FDA IDE Approval for Vascular ...
FDA IDE approved for the investigational xDot AMS. ✅ Pivotal study will enroll 266 patients, including roll-in subjects. ✅ Primary follow-up ...
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