Medical Products Agency
* A Multi-Centre, Double-Blind, Randomised, Placebo-Controlled Phase II Study to Assess the Effects on Atrial and Ventricular Refractoriness of an Intravenous Infusion of AZD2927 in Patients Undergoing an Invasive Electrophysiological Procedure. * The study has an adaptive design. In the 1st dose group the planned number of randomised patients is 24. The tentative number of randomised patients in the optional 2nd dose group is 12, 24 or 36 and thus a total maximum of 60 patients will be randomised in the study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
20
Research Site
Oslo, Norway
Research Site
Linköping, Sweden
Research Site
Örebro, Sweden
Research Site
Stockholm, Sweden
Research Site
Umeå, Sweden
Left Atrial Effective Refractory Period
Change in LAERP from before IP infusion to 1st and 2nd assessments during IP infusion
Time frame: Baseline to last assessment during IP infusion
Ventricular Effective Refractory Period
Change in VERP from before IP infusion to 1st and 2nd assessments during IP infusion
Time frame: Baseline to last assessment during IP infusion
Paced QT Interval
Change in CS Paced QT interval (P600 MS) from before and after IP infusion during electrophysiological measurements
Time frame: Baseline to last assessment during IP infusion
Atrio-ventricular Effective Refractory Period
Change from observation before IP infusion to during 1st and 2nd LAERP Mean
Time frame: Baseline to last assessment during IP infusion
PA Interval
Reflects intra-atrial conduction and is defined as the interval from the onset of the P wave in the surface ECG to the onset of atrial activation (A) in the His bundle electrogram. Change from observation before IP infusion to 30 min after IP start
Time frame: Baseline to last assessment during IP infusion
AH Interval
Change from observation before IP infusion to 30 mins after IP start. AH interval- the conduction time from the low right atrium at the inter-atrial septum through the AV node to the His bundle, ie, intra-nodal conduction time.
Time frame: Baseline to last assessment during IP infusion
HV Interval
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Change from observation before IP infusion to 30 mins after IP start. HV interval - represents conduction time from the proximal His bundle to the ventricular myocardium, ie, infra-nodal conduction time.
Time frame: Baseline to last assessment during IP infusion
PR Interval
Interval from the onset of the P-wave to the start of the QRS complex. Change from observation before IP infusion to 6 to 8 hours and 20 to 24 hours after IP infusion
Time frame: Baseline to last assessment during IP infusion
QRS Duration
Change from observation before IP infusion to 6 to 8 hours and 20 to 24 hours after IP infusion
Time frame: Baseline to last assessment during IP infusion
RR Interval
Change from observation before IP infusion to 6 to 8 hours and 20 to 24 hours after IP infusion
Time frame: Baseline to last assessment during IP infusion