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Malnutrition Assessment Tools in Surgery (MATS)

U

University Hospital of Crete

Status

Completed

Conditions

Malnutrition
Surgery--Complications

Study type

Observational

Funder types

Other

Identifiers

NCT05393752
18981/4-11-2021

Details and patient eligibility

About

The purpose of this study is to evaluate the main malnutrition risk assessment tools in patients undergoing operations of general surgery.

Full description

This is a multi centre prospective observational study including patients undergoing major/major+ operation of general surgery. Patients will be interviewed by surgical trainees and their malnutrition risk will be assessed with the use of SGA, MUST, NRS, MNA-SF etc. Clinical variables and demographics will also be recorded in order to enable meaningful comparisons of malnutrition risk assessment tools in terms of serious postoperative complications.

Enrollment

1,650 patients

Sex

All

Ages

18 to 108 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age >18 years

  • Patients undergoing elective or emergency surgery. Urgency of emergent operations is classified as follows, according to the clinical judgment of the surgeon, regarding the maximum time a patient could wait for surgery:

    • 3.Expedited (>18 hours)
    • 2B. Urgent (6-18 hours)
    • 2A. Urgent (2-6 hours)
      1. Immediate (<2 hours)
  • Operations involving the gastrointestinal tract

  • Magnitude of operation graded by POSSUM [17,18]:

    • Major+ (examples include colonic resection abdominoperineal resection of the rectum, radical total gastrectomy, intestinal bypass, whipple resection)
    • Major (examples include adhesiolysis, stoma formation, small bowel resection, anterior resection, cholecystectomy and exploration of the bile duct)

Exclusion criteria

  • Age <18 years

  • Magnitude of operation graded by POSSUM:

    • Minor
    • Intermediate
  • Inability to perform nutritional assessment

  • Inability to provide informed consent

Trial contacts and locations

2

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Central trial contact

Georgia Petra, MD, PhDc; Konstantinos Lasithiotakis, MD, PhD

Data sourced from clinicaltrials.gov

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