Recording and Evaluating Preoperative Malnutrition in Electively Scheduled Adult Surgical Patients With the GLIM Criteria (GLIM-study)
GLIM
1 other identifier
observational
215
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 17, 2023
CompletedFirst Posted
Study publicly available on registry
November 22, 2023
CompletedStudy Start
First participant enrolled
January 8, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 8, 2024
CompletedJanuary 30, 2025
January 1, 2025
3 months
November 17, 2023
January 28, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
prevalence of preoperative malnutrition
To study the prevalence of preoperative malnutrition according to the GLIM criteria in electively scheduled adult surgical patients.
preoperative
Interventions
prevalence of preoperative malnutrition
Eligibility Criteria
The study population will consist of electively scheduled adult surgical patients at the Amsterdam UMC, location AMC.
You may qualify if:
- 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
You may not qualify if:
- Patients \< 18 years
- Not speaking Dutch
- Patients who do not sign consent for re-use of care data
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Amsterdam UMC
Amsterdam, North Holland, 1105 AZ, Netherlands
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jeroen Hermanides, prof. dr.
j.hermanides@amsterdamumc.nl
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof dr.
Study Record Dates
First Submitted
November 17, 2023
First Posted
November 22, 2023
Study Start
January 8, 2024
Primary Completion
April 1, 2024
Study Completion
April 8, 2024
Last Updated
January 30, 2025
Record last verified: 2025-01