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The Feasibility Study of Dual-Section Nasogastric Tube

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01649349
First Posted: July 25, 2012
Last Update Posted: July 25, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Tsung Ju Wu, Changhua Christian Hospital
June 29, 2012
July 25, 2012
July 25, 2012
May 2012
June 2012   (Final data collection date for primary outcome measure)
Number of Participants with Adverse Events [ Time Frame: 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.
Same as current
No Changes Posted
satisfaction of Dual-Section Nasogastric Tube [ Time Frame: participants will be followed for the duration of hospital stay, an expected average of 1 weeks ]
using Likert scale for overall satisfaction
Same as current
Not Provided
Not Provided
 
The Feasibility Study of Dual-Section Nasogastric Tube
The Feasibility Study of Dual-Section Nasogastric Tube in Dysphagia Patients
The purpose of this studyis to assess the feasibility and safety of novel designed two-piece nasogastric tube.
Not Provided
Interventional
Early Phase 1
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
  • Stroke
  • Mouth Neoplasms
Device: two-piece nasogastric tube
one week period
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
10
June 2012
June 2012   (Final data collection date for primary outcome measure)

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
Sexes Eligible for Study: All
20 Years to 80 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
 
NCT01649349
110807
TW201010751 ( Registry Identifier: DUAL-SECTION NASOGASTRIC TUBE )
Not Provided
Not Provided
Not Provided
Tsung Ju Wu, Changhua Christian Hospital
Changhua Christian Hospital
Not Provided
Not Provided
Changhua Christian Hospital
July 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP