ClinicalTrials.Veeva

Menu

Home Monitoring Vs. Hospitalization for Mild Acute Pancreatitis (RHINO)

C

Catalan Institute of Health

Status

Enrolling

Conditions

Acute Pancreatitis

Treatments

Other: Experimental
Other: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT05473260
RHINO-TRIAL

Details and patient eligibility

About

Acute pancreatitis accounts for a large number of hospital admissions every year. Some studies have shown that early oral feeding protocols are safe, and one previous study suggests the possibility of home care for mild acute pancreatitis.

Full description

Approximately 80% of all cases of acute pancreatitis are mild and only require supportive care for pain and nausea control and an adequate fluid replacement. Currently, all patients in our setting diagnosed with mild acute pancreatitis are admitted to a conventional hospitalization ward under the supervision of the Digestive and General Surgery Department or the Gastroenterology Department. Symptomatic treatment is administered, and abdominal ultrasound is performed to assess the cause of pancreatic inflammation. The remaining 20% fulfill the severity criteria from its onset onwards and require intensive care support.

We will conduct a multicenter randomized controlled clinical trial to compare two different approaches to mild non-alcoholic acute pancreatitis: hospital admission and outpatient management.

Enrollment

308 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

INCLUSION CRITERIA

Patients diagnosed with mild acute pancreatitis based on at least two of the three following criteria:

  • Abdominal pain
  • Amylase or lipase 3x ULN (in blood/urine)
  • Imaging tests (Ultrasound/CT scan) suggestive of acute pancreatitis.

Age ≥18 years and <80 years

Absence of potential pancreatitis-related severity criteria:

  • No evidence of SIRS in the emergency room
  • C-Reactive Protein levels <150mg/dL
  • Marked increase in the White Blood Cell Count
  • Absence of coagulopathy (INR <1.4)
  • Hematocrit < 44%
  • Creatinine < 170 µmol/L
  • BISAP score ≤2 at the time of randomization.

Patients with good pain response to 12-hour supportive care in the ER (VAS <4) or adequate oral feeding tolerability.

Absence of local or systemic complications of acute pancreatitis on imaging tests.

Adequate cognitive capacity and without any previous diagnose of psychiatric disease.

Patients who meet each participating hospital home care criteria. Patients who give their written informed consent to participate.

EXCLUSION CRITERIA

Past medical history of pancreatic disease:

  • Known or newly diagnosed chronic pancreatitis (Wirsung dilation or pancreatic calcifications in previous imaging tests)
  • Patients with recurrent acute pancreatitis (>3 episodes/year) or an episode of acute pancreatitis <1 month ago.
  • Acute pancreatitis after endoscopic retrograde cholangiography.
  • Hyperbilirubinemia >3x ULN

Comorbidities that required previous hospitalization (myocardial infarction, liver cirrhosis, chronic kidney disease, or chronic lung disease).

BMI ≥35 Kg/m2 Patients who refuse to participate in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

308 participants in 2 patient groups

HOSPI Group
Active Comparator group
Description:
Patients with mild acute pancreatitis randomized to in-hospital care.
Treatment:
Other: Control
HOME Group
Experimental group
Description:
Patients with mild acute pancreatitis randomized to early discharge and outpatient clinic follow-up.
Treatment:
Other: Experimental

Trial contacts and locations

1

Loading...

Central trial contact

Juli Busquets, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems