The Feasibility Study of Dual-Section Nasogastric Tube

NCT ID: NCT01649349

Last Updated: 2012-07-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

EARLY_PHASE1

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-05-31

Study Completion Date

2012-06-30

Brief Summary

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

Detailed Description

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Conditions

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Stroke Mouth Neoplasms

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Interventions

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two-piece nasogastric tube

one week period

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

20 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Changhua Christian Hospital

OTHER

Sponsor Role lead

Responsible Party

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Tsung Ju Wu

M.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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TW201010751

Identifier Type: REGISTRY

Identifier Source: secondary_id

110807

Identifier Type: -

Identifier Source: org_study_id