This prospective randomized controlled trial was designed to evaluate whether the M1/M3-selective antagonist penehyclidine hydrochloride could more effectively reverse pediatric microcirculatory dysfunction than traditional atropine, particularly when macrohemodynamics appear normalized.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
98
atropine control group
penehyclidine hydrochloride
Guangzhou Women and Children's Medical Center
Guangzhou, Guangdong, China
the duration of CRT(capillary refill time)
Time frame: 7 days
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