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NCT05936996: ACCESS MANTA

Prospective Clinical Registry Evaluating Contemporary MANTA Outcomes

Completed Last updated 12 November 2025
What this trial tests

trial testing MANTA Vascular Closure Device in Femoral Arteriotomy Closure in 258 participants. Completed in 30 October 2025.

Timeline
15 November 2023
Primary endpoint
20 June 2025
30 October 2025

Quick facts

Lead sponsorEssential Medical, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment258
Start date15 November 2023
Primary completion20 June 2025
Estimated completion30 October 2025
Sites10 locations across Canada, United States

Drugs / interventions tested

Conditions studied

Sponsor

Essential Medical, Inc.

Who can join

21 and older, any sex, with Femoral Arteriotomy Closure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is an observational study designed to evaluate the safety and clinical outcomes of the MANTA® Vascular Closure Device (VCD) (the MANTA® Device) in TAVR procedures. The study will enroll participants who are undergoing a TAVR procedure. The purpose of this study is to examine and collect data on outcomes of contemporary MANTA® large bore closure in standard of care (SOC) TAVR procedures with on-label use of the MANTA® device including appropriate patient selection and proper vascular access.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of MANTA Vascular Closure Device

Trials testing the same drug.

Other recruiting trials for Femoral Arteriotomy Closure

Currently open trials in the same condition.

Other Essential Medical, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05936996.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing