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Prognostic Value of Different Nutritional Screening Tools in Acute Pancreatitis (NuRiPa)

U

University Medicine Greifswald

Status

Active, not recruiting

Conditions

Malnutrition
Acute Pancreatitis

Treatments

Other: No intervention - observational study only

Study type

Observational

Funder types

Other

Identifiers

NCT05613673
BB 112/22

Details and patient eligibility

About

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.

Full 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.

Enrollment

110 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • verified diagnosis of acute pancreatitis
  • provision of informed consent

Exclusion criteria

  • pregnancy
  • inability to provide consent

Trial contacts and locations

1

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Central trial contact

Ali A Aghdassi, Professor

Data sourced from clinicaltrials.gov

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