한국 탐색적 임상시험

완료한 임상 시험 (First-in-man study)

디넥스 시스템은 탐색적 임상시험에서 안정성과 유효성이 확인되었습니다. (논문 게재)

DETAILS
Enrollment 16 participants.
Allocation N/A (Single-Arm).
Masking None (Open Label).
# of trial centers 4 (multi).
Inclusion criteria Office SBP > 150 mmHg.
Daytime AMSBP > 140 mmHg.
> 3 anti-HTN meds incl. diuretics.
RESULTS
Safety issue None
Procedure time 20.3 + 10.9 minutes
(Min. 12 minutes, Max. 45 minutes).
DENEX Pilot Study: NCT04248530
더 알아보기
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