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Not listed No phase listed Observational

AMBULATE Same Day Discharge Registry

ClinicalTrials.gov ID: NCT04203329

Public ClinicalTrials.gov record NCT04203329. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 10:58 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-center, Prospective, Single Arm Registry to Evaluate Procedural Outcomes Using the Cardiva VASCADE MVP VVCS Closure Device After Catheter-based Atrial Fibrillation Interventions for Patients Who Are Discharged the Same Day.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A multi-center, prospective, single-arm post market registry, designed to collect both performance and complication outcomes when same day discharge is enabled by the study device, in sealing multiple femoral venous access sites at the completion of ablation procedures for atrial fibrillation with or without another arrhythmia, performed through 6 - 12 Fr inner diameter (maximum 15F OD) introducer sheaths.

Study identification

NCT ID
NCT04203329
Recruitment status
Not listed
Study type
Observational
Phase
Not listed
Lead sponsor
Cardiva Medical, Inc.
Industry
Enrollment
700 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2020 (Actual)
Primary completion
Dec 2023 (Estimated)
Completion
Dec 2023 (Estimated)
Last update posted
Aug 10, 2022

2020 – 2023

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
University of Alabama Birmingham Birmingham Alabama 35233 —
HonorHealth Scottsdale Arizona 85260 —
Coastal Cardiology San Luis Obispo California 93401 —
Aurora Denver Cardiology Associates, The Medical Center of Aurora Aurora Colorado 80012 —
MedStar Washington Washington D.C. District of Columbia 20010 —
Emory St. Joseph's Hospital Atlanta Georgia 30342 —
Lahey Clinic Burlington Massachusetts 01805 —
Valley Hospital Ridgewood New Jersey 07450 —
Wake Med Hospital Raleigh North Carolina 27610 —
Cleveland Clinic Cleveland Ohio 44195 —
Texas Cardiac Arrhythmia Institute Austin Texas 78705 —
Medical City Dallas Hospital Dallas Texas 75230 —
Medical City Fort Worth Fort Worth Texas 76104 —
University of Utah Health Salt Lake City Utah 84132 —
Chippenham Hospital Richmond Virginia 23225 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04203329, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 10, 2022 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04203329 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →