Comparing nutritional screening tools for liver cirrhosis patients
Comparison of Two Nutritional Screening Tools for the Detection of Malnutrition in Patients with Liver Cirrhosis
This study is testing two special questionnaires to see which one better helps find malnutrition in people with liver cirrhosis.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 46 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | Hospital Clinic of Barcelona Academic / other |
| Locations | 1 site (Barcelona, Catalonia) |
| Trial ID | NCT04502719 on ClinicalTrials.gov |
What this trial studies
This study evaluates two nutritional screening questionnaires specifically designed for patients with liver cirrhosis. All participants will undergo assessments using both questionnaires alongside a complete nutritional evaluation. The goal is to improve the identification of malnutrition in these patients, which is crucial for enhancing clinical outcomes and quality of life. By utilizing these tailored screening tools, the study aims to address the challenges posed by traditional methods that may not be suitable for cirrhotic patients.
Who should consider this trial
Good fit: Ideal candidates for this study are patients diagnosed with liver cirrhosis.
Not a fit: Patients with cognitive impairment or major psychiatric disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved identification and treatment of malnutrition in liver cirrhosis patients, enhancing their overall health outcomes.
How similar studies have performed: Other studies have shown that tailored nutritional screening tools can significantly improve the identification of malnutrition in specific patient populations, suggesting a promising approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients diagnosed with liver cirrhosis. Exclusion Criteria: * Patients with cognitive impairment or major psychiatric disorder. * Lack of consent from the patient for inclusion in the study. * Any patient who is not suitable based on the researcher's own judgement.
Where this trial is running
Barcelona, Catalonia
- Hospital Clinic de Barcelona — Barcelona, Catalonia, Spain (Recruiting)
Study contacts
- Principal investigator: Joan Trabal, RDN, PhD — Hospital Clinic of Barcelona
- Study coordinator: Joan Trabal, RDN, PhD
- Email: jtrabal@clinic.cat
- Phone: +342275400
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.