- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06144411
Recording and Evaluating Preoperative Malnutrition in Electively Scheduled Adult Surgical Patients With the GLIM Criteria (GLIM-study) (GLIM)
April 15, 2024 updated by: B Preckel, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
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.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
700
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: E S de Klerk, drs.
- Phone Number: +31 (0)20 - 5662533
- Email: e.s.deklerk@amsterdamumc.nl
Study Contact Backup
- Name: Mireille FM van Stijn, MD. PhD
- Phone Number: +31 (0)20 - 5662533
- Email: m.f.vanstijn@amsterdamumc.nl
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
The study population will consist of electively scheduled adult surgical patients at the Amsterdam UMC, location AMC.
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
prevalence of preoperative malnutrition
Time Frame: preoperative
|
To study the prevalence of preoperative malnutrition according to the GLIM criteria in electively scheduled adult surgical patients.
|
preoperative
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jeroen Hermanides, prof. dr., j.hermanides@amsterdamumc.nl
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
June 1, 2024
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
July 1, 2026
Study Registration Dates
First Submitted
November 17, 2023
First Submitted That Met QC Criteria
November 17, 2023
First Posted (Actual)
November 22, 2023
Study Record Updates
Last Update Posted (Actual)
April 16, 2024
Last Update Submitted That Met QC Criteria
April 15, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023.0890
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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