NCT02599636

Brief Summary

Many factors before and after ICU stay determine the outcome of patients at ICU discharge, the type of illness, physical dependence and other sequelae can be a trigger for complications in hospital ward which can induce ICU readmission and worse outcome. The quality of medical assistance during all the hospitalisation should be guaranteed and many complications or fatal events could be avoidable. The objective of the present study is to demonstrate that collaboration between the intensivist and other medical teams in ward can reduce ICU readmission and hospital mortality after ICU discharge.

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
1,200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2015

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

October 1, 2015

Completed
29 days until next milestone

First Submitted

Initial submission to the registry

October 30, 2015

Completed
7 days until next milestone

First Posted

Study publicly available on registry

November 6, 2015

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2016

Completed
Last Updated

July 14, 2016

Status Verified

July 1, 2016

Enrollment Period

11 months

First QC Date

October 30, 2015

Last Update Submit

July 13, 2016

Conditions

In-Hospital MortalityNumber of ICU ReadmissionNumber of Warnings On-duty

Outcome Measures

Primary Outcomes (1)

  • The decline in hospital mortality

    3 months

Secondary Outcomes (1)

  • The decline in number of warnings on-duty

    3 months

Interventions

None interventionOTHER

Investigators will study the usual medical assistance

Eligibility Criteria

Age18 Years - 99 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients at ICU discharge

You may qualify if:

  • All patients with Sabadell Score 1 (poor prognosis in long term) and 2 (poor prognosis in short term) at ICU discharge

You may not qualify if:

  • patients younger than 18 years old
  • patients with Sabadell Score 0 (good prognosis)
  • patients with Sabadell Score 3 (null expected survival)
  • patients transferred to other hospitals

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Althaia Xarxa Assistencial Universitaria de Manresa

Manresa, Barcelona, 08243, Spain

Location

Study Officials

  • Silvia Cano Hernández, Physician

    Althaia Xarxa Assistencial Universitaria de Manresa

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physician

Study Record Dates

First Submitted

October 30, 2015

First Posted

November 6, 2015

Study Start

October 1, 2015

Primary Completion

September 1, 2016

Study Completion

September 1, 2016

Last Updated

July 14, 2016

Record last verified: 2016-07

Locations

ES(1)