The Feasibility Study of Dual-Section Nasogastric Tube

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Tsung Ju Wu, Changhua Christian Hospital
ClinicalTrials.gov Identifier:
NCT01649349
First received: June 29, 2012
Last updated: July 22, 2012
Last verified: July 2012

June 29, 2012
July 22, 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 ] [ Designated as safety issue: Yes ]
monitor the adverse events like pressure sore, numbers of self-extubation, dislocation of tube, or other unpredictable events.
Same as current
Complete list of historical versions of study NCT01649349 on ClinicalTrials.gov Archive Site
satisfaction of Dual-Section Nasogastric Tube [ Time Frame: participants will be followed for the duration of hospital stay, an expected average of 1 weeks ] [ Designated as safety issue: No ]
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
Phase 0
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: 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
Both
20 Years to 80 Years
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT01649349
110807, TW201010751
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