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Active Not RecruitingNCT05613673

Prognostic Value of Different Nutritional Screening Tools in Acute Pancreatitis

Comparison of the Prognostic Value of Different Nutritional Assessment Scores Regarding the Course in Acute Pancreatitis - a Prospective Trial

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
110 (estimated)
Sponsor
University Medicine Greifswald · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

The goal of this observational study is to compare the prognostic value of different nutritional screening tools to predict the course of acute pancreatitis. The main questions it aims to answer are: * Which nutritional screening tool performs best to predict length of hospital stay? * Which nutritional screening tool performs best to predict clinical outcome (disease severity, length of hospital stay, mortality, need for rehospitalization)? Participants will answer questions regarding their nutritional status and undergo basic anthropometric assessments (e.g. measurement of waist circumference) to evaluate their risk of malnutrition.

Detailed description

Malnutrition seems to be related to an adverse outcome of acute pancreatitis. However, it is still unclear which of the various available nutritional screening tools is suited best to predict the clinical outcome in hospitalized patients with acute pancreatitis. Therefore, in this study we compare the predictive performance of 6 different nutritional screening tools that are commonly applied in clinical practice regarding their respective associations with severity of acute pancreatitis, length of hospital stay, mortality and need for rehospitalization. To determine patients' nutritional status, subjects will be inquired about their recent food intake as well as body weight and undergo basic anthropometric assessments according to the different screening tools. Six months after the initial diagnosis patients will be contacted via mail to report on need for rehospitalization due to acute pancreatitis during this time period.

Conditions

Interventions

TypeNameDescription
OTHERNo intervention - observational study onlyNo intervention - observational study only

Timeline

Start date
2022-10-11
Primary completion
2024-10-05
Completion
2025-04-05
First posted
2022-11-14
Last updated
2024-12-27

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT05613673. Inclusion in this directory is not an endorsement.