The purpose of this studyis to assess the feasibility and safety of novel designed two-piece nasogastric tube.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
10
one week period
Number of Participants with Adverse Events
monitor the adverse events like pressure sore, numbers of self-extubation, dislocation of tube, or other unpredictable events.
Time frame: participants will be followed for the duration of hospital stay, an expected average of 1 weeks
satisfaction of Dual-Section Nasogastric Tube
using Likert scale for overall satisfaction
Time frame: participants will be followed for the duration of hospital stay, an expected average of 1 weeks
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