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Recruiting NCT06648551

Diagnostic Performance of Controlling Nutritional Status as a Nutritional Screening Tool in Patients With Inflammatory Bowel Disease

Observational Inflammatory Bowel Disease 5

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: CONUT.
Who it may be relevant to
Registry conditions: Inflammatory Bowel Disease 5. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Mexico
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Diagnostic Performance of CONUT as a Nutritional Screening Tool in Patients With Inflammatory Bowel Disease

Overview

The objective of this observational study is to determine the diagnostic performance of CONUT as a nutritional screening tool in patients with Inflammatory Bowel Disease. The main questions to be answered are: What is the sensitivity and specificity of CONUT as a nutritional screening tool in patients with Inflammatory Bowel Disease? The participants will: Undergo body composition analysis and a medical history review to understand the characteristics of their current condition, apply the GLIM criteria, and conduct their nutritional assessment.

Interventions

  • Diagnostic test CONUT
    It is a scale that uses albumin, lymphocytes, and cholesterol for the diagnosis of malnutrition

Primary outcome measures

  • Diagnostic test [Time frame: one year]

Eligibility criteria

Inclusion criteria

  • Age 18 years and older
  • Gender unspecified
  • Histologically confirmed Ulcerative Colitis
  • Diagnosis confirmed by a specialist physician

Exclusion criteria

  • Patients with any amputation or prosthesis
  • Patients with a pacemaker
  • Patients with any neoplasm
  • Pregnancy or lactation
  • With comorbidities such as diabetes, hypertension, heart failure, thyroid problems

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Mexico · 1 center
  • Nallely Hernandez Bueno — Mexico City

Identifiers

NCT: NCT06648551 · DI/23/501/03/31

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗