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Trials / Unknown

UnknownNCT05462769

Percutaneous Plug-based Arteriotomy Closure Device Use in Minimally Invasive Cardiac Surgery

Status
Unknown
Phase
Study type
Observational
Enrollment
600 (estimated)
Sponsor
Karolinska University Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

A single-center prospective study. Patients undergoing minimally invasive cardiac surgery between 2017 and 2022 at the Karolinska University Hospital in Stockholm, Sweden are eligible. Femoral cannulation was performed percutaneously with planned percutaneous arteriotomy closed using a plug-based arteriotomy closure device (MANTA; Teleflex/Essential Medical, Malvern, PA). Data regarding preoperative clinical characteristics and operative details were obtained by medical records review.

Conditions

Interventions

TypeNameDescription
DEVICEPercutaneous vascular closurePercutaneous arteriotomy closed using a plug-based arteriotomy closure device

Timeline

Start date
2017-08-01
Primary completion
2022-12-01
Completion
2022-12-01
First posted
2022-07-18
Last updated
2022-07-18

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT05462769. Inclusion in this directory is not an endorsement.

Percutaneous Plug-based Arteriotomy Closure Device Use in Minimally Invasive Cardiac Surgery (NCT05462769) · Clinical Trials Directory