NCT04088825

Brief Summary

Nutrition Department of University Hospital La Paz decided to implement some method of screening in our centre which allowed us to detect as many patients with malnutrition risk as possible. Due to the large size of our centre, with about 1,500 beds and the few human resources in our unit, we chose to use the CONUT system (Nutritional Control), a 100% automatic method based on analytical parameters, very easy to use, low cost and whose validity is confirmed, characteristics that fulfilled our needs. The implementation of this nutritional screening method has led to a change in the ìnutritionafi culture of our centre respect to DRM in most of our professionals: doctors and nurses and even in the management team, so all of them understand the importance of the process and know about the available tools and knowledge to indicate an adequate and early nutritional support.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
233

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2012

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

July 15, 2012

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 15, 2012

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2012

Completed
6.7 years until next milestone

First Submitted

Initial submission to the registry

September 12, 2019

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 13, 2019

Completed
Last Updated

September 13, 2019

Status Verified

August 1, 2019

Enrollment Period

2 months

First QC Date

September 12, 2019

Last Update Submit

September 12, 2019

Conditions

Outcome Measures

Primary Outcomes (1)

  • To detect as many patients with malnutrition risk as possible

    The method collects information from databases of Admission Service (affiliation, age, date) and Laboratory (albumin, cholesterol, total lymphocytes) and generates, in the report of analytical results, "alert" information about each patient's nutritional risk and also nutritional recommendations based on the risk identified. Prior to its implantation several evaluations were performed in order to allow us to better know the extra workload, as it was the main factor that could limit our ability to assume that screening method and also many training activities for doctors and hospital health professionals who were increasingly assuming responsibilities in the nutritional treatment of their patients.

    Three months

Interventions

CONUT has been working from june of 2010 and it has detected risk of malnutrition in 32% of the evaluated patients. The method collects information from databases of Admission Service (affiliation, age, date) and Laboratory (albumin, cholesterol, total lymphocytes) and generates, in the report of analytical results, "alert" information about each patient's nutritional risk and also nutritional recommendations based on the risk identified.

Eligibility Criteria

Age15 Years+
Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Cross-sectional study in which the nutritional status of patients will be assessed in the first 72 hours of entry.

You may qualify if:

  • Patients of both sexes
  • Patients older than 15 years
  • Patients admitted to the General Hospital or Traumatology area
  • Patients who have signed the informed consent to participate in the study

You may not qualify if:

  • Pregnant women.
  • Patients whose physical and / or psychic capacity prevents them from providing all the data collected by the evaluated methods or who do not have a caregiver.
  • Non-collaborating patients in data collection
  • Patients in whom a hospital stay of less than 48 hours is expected.
  • Patients who at the time of performing the analyzes are in the ICU and OER

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Institute for Health Research IdiPAZ

Madrid, Spain

Location

MeSH Terms

Conditions

Malnutrition

Condition Hierarchy (Ancestors)

Nutrition DisordersNutritional and Metabolic Diseases

Study Officials

  • Carmen Gómez Candela, Msc

    Hospital Universitario La Paz

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 12, 2019

First Posted

September 13, 2019

Study Start

July 15, 2012

Primary Completion

September 15, 2012

Study Completion

December 31, 2012

Last Updated

September 13, 2019

Record last verified: 2019-08

Locations