Study of Normal Conditions of Use, Dosing, and Safety of Intravenous (IV) Administration of Vernakalant (MK-6621-049) : A Prospective Observational Registry Study to Characterise Normal Conditions of Use, Dosing and Safety Following Administration of Vernakalant IV Sterile Concentrate

This non-interventional prospective study is a post-authorization safety study (PASS) of vernakalant conducted to collect information about normal conditions of use and appropriate dosing, and to quantify possible medically significant risks associated with the use of vernakalant in real-world clinical practice..

Medienart:

Klinische Studie

Erscheinungsjahr:

2019

Erschienen:

2019

Enthalten in:

ClinicalTrials.gov - (2019) vom: 30. Dez. Zur Gesamtaufnahme - year:2019

Sprache:

Englisch

Links:

Volltext [kostenfrei]

Themen:

610
Atrial Fibrillation
Medical Condition: Atrial Fibrillation
Recruitment Status: Completed
Study Type: Observational

Anmerkungen:

Source: Link to the current ClinicalTrials.gov record., First posted: June 10, 2011, Last downloaded: ClinicalTrials.gov processed this data on June 14, 2021, Last updated: June 15, 2021

Study ID:

NCT01370629
6621-049
EP01029.004

Veröffentlichungen zur Studie:

fisyears:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

CTG001079549