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Baseline and new‐onset morphologic ECG abnormalities in healthy volunteers in phase I studies receiving placebo: Changes over a 6‐week follow‐up period
Author(s) -
Hingorani Pooja,
Karnad Dilip R.,
Natekar Mili,
Kothari Snehal,
Narula Dhiraj
Publication year - 2014
Publication title -
the journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.92
H-Index - 116
eISSN - 1552-4604
pISSN - 0091-2700
DOI - 10.1002/jcph.282
Subject(s) - medicine , sinus bradycardia , placebo , bradycardia , sinus tachycardia , qt interval , cardiology , electrocardiography , tachycardia , pr interval , u wave , heart rate , blood pressure , pathology , alternative medicine
Morphological ECG abnormalities occur in 5–12% healthy adults participating in early phase clinical trials. We retrospectively analyzed 16,472 12‐lead ECGs recorded at multiple time points in 420 volunteers (282 males, 138 females; aged 18–76 years) randomized to receive placebo from 19 Phase I studies to see if some baseline ECG abnormalities may disappear or new abnormalities may appear during the study. One hundred forty‐four (34.3%) subjects had abnormal baseline ECGs, of which 66 (44.8%) reverted to normal during follow‐up. Of 276 (65.7%) subjects with normal baseline ECGs, 118 (42.8%) developed ECG abnormalities over the next 6 weeks. Common baseline abnormalities included sinus bradycardia, R wave transition abnormalities, right axis deviation, non‐specific T wave changes and atrial premature complexes. On follow‐up ECGs, prolonged QT interval, first‐degree AV block, sinus bradycardia, short PR interval, and R wave transition abnormalities reverted to normal. Common new‐onset abnormalities in subjects with normal baseline ECGs included sinus bradycardia, prolonged QT interval, non‐specific T wave changes, R wave transition abnormalities, and sinus tachycardia. Thus, transient morphological ECG changes may occur in healthy volunteers possibly due to diurnal variation, effect of food, hormones, or autonomic changes. This should be considered when interpreting “treatment‐emergent” ECG changes in clinical trials.