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COMPLETED

AMBULATE VASCADE MVP Same Day Discharge Retrospective Registry

NCT04538781 · View on ClinicalTrials.gov ↗

Study Summary

A multi-center, retrospective, single arm post market registry to evaluate procedural outcomes data using the Cardiva VASCADE MVP Venous Vascular Closure System (VVCS) for the management of the femoral venotomy after catheter-based atrial fibrillation interventions with or without another arrythmia performed via 6-12F procedural sheaths with single or multiple access sites per limb for patients who are discharged the same day.

Conditions Studied

Interventions

  • DEVICE VASCADE MVP VVCS

Study Locations (4)

California

  • Coastal Cardiology — San Luis Obispo

District of Columbia

  • MedStar Washington — Washington D.C.

Massachusetts

  • Lahey Clinic — Burlington

Ohio

  • Cleveland Clinic — Cleveland

Trial Details

FieldValue
Enrollment Target 497 participants
Start Date 2020-10-09
Est. Completion 2021-02-08

Sponsor

Cardiva Medical

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04538781

The ClinicalTrials.gov registry entry for NCT04538781 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 497 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cardiva Medical, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Atrial Fibrillation appearing as the primary indexed condition, and to 1 intervention — of which VASCADE MVP VVCS is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04538781 reports 4 study locations spanning 4 distinct geographic areas — top geographies include California, District of Columbia, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04538781 about?

NCT04538781 is a clinical study titled "AMBULATE VASCADE MVP Same Day Discharge Retrospective Registry". A multi-center, retrospective, single arm post market registry to evaluate procedural outcomes data using the Cardiva VASCADE MVP Venous Vascular Closure System (VVCS) for the management of the femoral venotomy after catheter-based atrial fibrillation interventions with or without another arrythmia ...

What is the current status of trial NCT04538781?

This trial is currently completed. The enrollment target is 497 participants. The study started on 2020-10-09. Estimated completion is 2021-02-08.

What conditions does trial NCT04538781 study?

This clinical trial studies the following conditions: Atrial Fibrillation. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04538781?

The interventions under investigation include: VASCADE MVP VVCS (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04538781?

This trial is sponsored by Cardiva Medical, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04538781 being conducted?

This trial has 4 study locations across California, District of Columbia, Massachusetts, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial