The Feasibility Study of Dual-Section Nasogastric Tube

The Feasibility Study of Dual-Section Nasogastric Tube in Dysphagia Patients

Status

Completed

Phases

Early Phase 1

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01649349

Enrollment

Registered

2012-07-25

Start date

2012-05-31

Completion date

2012-06-30

Last updated

2012-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mouth Neoplasms, Stroke

Brief summary

The purpose of this studyis to assess the feasibility and safety of novel designed two-piece nasogastric tube.

Interventions

DEVICEtwo-piece nasogastric tube

one week period

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

20 Years to 80 Years

Healthy volunteers

Inclusion criteria

* dysphagia * mouth neoplasms * stroke * already use conventional nasogastric tube for at least 2 weeks

Exclusion criteria

* unconsciousness patient * unstable medical condition with needs of closely medical care * unable to fill in inform consent * the fixed length was less than 50 or more than 60 centimeter when using conventional nasogastric tube

Design outcomes

Primary

Measure	Time frame	Description
Number of Participants with Adverse Events	participants will be followed for the duration of hospital stay, an expected average of 1 weeks	monitor the adverse events like pressure sore, numbers of self-extubation, dislocation of tube, or other unpredictable events.

Secondary

Measure	Time frame	Description
satisfaction of Dual-Section Nasogastric Tube	participants will be followed for the duration of hospital stay, an expected average of 1 weeks	using Likert scale for overall satisfaction

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026