NCT01277393

Brief Summary

This study is to find out care of critically ill patients enteral nutrition guidelines for the implementation of the effectiveness of the intervention.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Sep 2010

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2010

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

January 12, 2011

Completed
2 days until next milestone

First Posted

Study publicly available on registry

January 14, 2011

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2011

Completed
Last Updated

January 14, 2011

Status Verified

January 1, 2011

First QC Date

January 12, 2011

Last Update Submit

January 12, 2011

Conditions

ICU Ill PatientsEnteral Nutrition Feeding

Keywords

Enteral nutrition feeding

Study Arms (2)

Experimental Group

Control Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

ill patients

You may qualify if:

  • ICU patients elder than 18 years of age
  • (APACHE II) score \> 15
  • Patients expected to remain in ICU for more than 2 days

You may not qualify if:

  • Patients that have consented to a Do-Not-Resuscitate document
  • Patients not expected survive more than 2 days
  • Patients that have returned to ICU due to their condition worsening after previously leaving ICU
  • Patients that have transferred from ICU of other hospitals.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Taipei Medical University - WanFang Hospital

Taipei, Taiwan

Location

Study Officials

  • Chin-Feng Huang

    Taipei Medical University WanFang Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

January 12, 2011

First Posted

January 14, 2011

Study Start

September 1, 2010

Study Completion

March 1, 2011

Last Updated

January 14, 2011

Record last verified: 2011-01

Locations

TW(1)