Clinical trial · Interventional

The Feasibility Study of Dual-Section Nasogastric Tube

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

NCT01649349CI-TRIAL-00007557completedEarly Phase 1ClinicalTrials.gov clinicaltrialsPublishedExplore in graph →

Summary

Brief summary (as posted)

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

Conditions

Conditions (2)

Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.

Condition (as posted)	Mapped entity	Match	Confidence
Mouth Neoplasms	Oral Cavity Neoplasm	ALIAS	0.90
Stroke	—	UNRESOLVED	—

Interventions

Interventions (1)

Intervention	Type	Mapped drug	Match
two-piece nasogastric tube	Device	—	UNRESOLVED

Design

Arms and outcomes

Arms (0)

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Primary outcomes (1)

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

Secondary outcomes (1)

measure
satisfaction of Dual-Section Nasogastric Tube
timeFrame
participants will be followed for the duration of hospital stay, an expected average of 1 weeks
description
using Likert scale for overall satisfaction

Eligibility

Eligibility (as posted)

Sex: All
Minimum age: 20 Years
Maximum age: 80 Years

Show eligibility criteria text

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

References

Publications (0)

Data not yet available

No reference posted for this study.