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Recording and Evaluating Preoperative Malnutrition in Electively Scheduled Adult Surgical Patients With the GLIM Criteria (GLIM-study)

Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06144411
Collaborator
(none)
700
Enrollment
5.7
Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

Data about the prevalence of preoperative malnutrition according to all the five GLIM criteria among the broad range of surgical patients are lacking. The current study will investigate the prevalence of malnutrition according to all of the five GLIM criteria in electively planned surgical patients in a large academic hospital, the Amsterdam University Medical Centres, location AMC, where over 11.000 patients are operated on yearly.

Condition or Disease Intervention/Treatment Phase
  • Other: prevalence of preoperative malnutrition

Study Design

Study Type:
Observational
Anticipated Enrollment :
700 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Recording and Evaluating Preoperative Malnutrition in Electively Scheduled Adult Surgical Patients With the GLIM Criteria (GLIM-study)
Anticipated Study Start Date :
Jan 8, 2024
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
Jul 1, 2024

Outcome Measures

Primary Outcome Measures

  1. prevalence of preoperative malnutrition [preoperative]

    To study the prevalence of preoperative malnutrition according to the GLIM criteria in electively scheduled adult surgical patients.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:

  • Patients scheduled for elective surgery at the operating theatres of the AUMC, location AMC

  • Patients ≥ 18 years

  • Dutch speaking

  • Willing and able to sign consent for re-use of care data

  • The study can be combined with other studies

Exclusion Criteria:

  • Patients < 18 years

  • Not speaking Dutch

  • Patients who do not sign consent for re-use of care data

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Investigators

  • Principal Investigator: Jeroen Hermanides, prof. dr., j.hermanides@amsterdamumc.nl

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
B Preckel, Prof dr., Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
ClinicalTrials.gov Identifier:
NCT06144411
Other Study ID Numbers:
  • 2023.0890
First Posted:
Nov 22, 2023
Last Update Posted:
Nov 22, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Malnutrition

Study Results

No Results Posted as of Nov 22, 2023