Condition category
Digestive System
Date applied
Date assigned
Last edited
Prospectively registered
Overall trial status
Recruitment status
Not yet recruiting

Plain English Summary

Background and study aims
The pancreas is an organ in the upper abdomen sitting below the stomach. Its function is to produce enzymes to digest food, as well as producing hormones to control blood sugars. When the pancreas becomes inflamed it can cause pain and sickness, as well as affecting other vital organs. This condition is termed acute pancreatitis. The severity of acute pancreatitis can range from being mild to very severe where some patients spend a long time in hospital. Acute pancreatitis is treated mainly by rehydration, as well as giving pain relief and anti-sickness medications. The inflammation usually settles on its own. However, for the small minority of patients who are unfortunate to develop a severe form of acute pancreatitis, bacterial infection around the pancreas can be a problem, and this may require additional treatment such as antibiotics. Telling the difference between inflammation and bacterial infection in acute pancreatitis can be difficult. Both conditions can cause a fever and a fast heart rate. Antibiotics are often prescribed where there is no bacterial infection, so there will be no benefit to patients, but can cause harmful side-effects such as severe diarrhea and inflammation of the bowel. There is also a risk of developing bacteria that are resistant to common antibiotics, limiting the choice of antibiotics if they are needed in the future. It is therefore important to only give antibiotics to those patients who have a bacterial infection. There are blood tests, such as Procalcitonin, that can help to distinguish between inflammation and infection. The aim of this study is to see how effective Procalcitonin is at guiding doctors in using antibiotics in acute pancreatitis. Procalcitonin is produced by the cells in our body in response to infection. This can be measured in blood samples. At the moment, it can be used to guide antibiotic treatment in common conditions such as chest infections. Its role for patients with acute pancreatitis who are suspected of having infection, however, is not yet clear.

Who can participate?
Patients aged over 18 with acute pancreatitis

What does the study involve?
Participants are randomly allocated to receive antibiotics either in response to a procalcitonin algorithm or by standard decision making. All other aspects of the care of patients are the same. The study assesses whether the use of procalcitonin measurement allows for a reduction in the use of antibiotics without compromising patient outcome.

What are the possible benefits and risks of participating?
There is evidence from other studies that the use of procalcitonin measurement to guide antibiotic use results in more appropriate use of antibiotics. There are not likely to be any risks from participation.

Where is the study run from?
Manchester Royal Infirmary (UK)

When is the study starting and how long is it expected to run for?
January 2017 to October 2020

Who is funding the study?
Manchester University NHS Foundation Trust (UK)

Who is the main contact?
Prof. Ajith Siriwardena

Trial website

Contact information



Primary contact

Prof Ajith Siriwardena


Contact details

Regional Hepato-Pancreato-Biliary Service
Department of Surgery
Manchester Royal Infirmary
Oxford Road
M13 9WL
United Kingdom

Additional identifiers

EudraCT number number

Protocol/serial number

Version 1.0

Study information

Scientific title

PROCalcitonin-based algorithm for antibiotic use in Acute Pancreatitis: a randomised controlled trial



Study hypothesis

This study tests the hypothesis that a procalcitonin-based algorithm to guide initiation, continuation and discontinuation of antibiotics will lead to reduced antibiotic use in patients with acute pancreatitis without an adverse effect on outcome.

Ethics approval

Not provided at time of registration

Study design

Single-centre randomised controlled single-blind two-arm phase III pragmatic clinical and cost-effectiveness trial

Primary study design


Secondary study design

Randomised controlled trial

Trial setting


Trial type


Patient information sheet

Not available in web format, please use the contact details to request a patient information sheet


Acute pancreatitis


Method of randomisation:
Web-based randomisation will be provided by the Clinical Trials Unit of the University of Edinburgh ( Allocation will be in a ratio of 1:1 to routine or algorithm-guided care. Randomization will be stratified by severity (mild or moderately severe/severe) and admission pathway (whether or not the patient has their index (first) admission with acute pancreatitis to the Manchester Royal Infirmary [direct] or is transferred from another hospital [tertiary transfer]). A random block size of 4, 6 or 8 will be applied to each stratum.

Patients will be randomly allocated to receive antibiotics either in response to a procalcitonin algorithm or by standard decision making. All other aspects of the care of patients will be the same. The main endpoint is whether the use of procalcitonin measurement allows for a reduction in use of antibiotics without compromising outcome.

Summary methodology for intervention arm:
The intervention is the use of a procalcitonin-based algorithm to guide antibiotic use. The algorithm is a simplified, bi-modal guide: consider antibiotic use if PCT >1 ng/mL, do not use if PCT below this point. Patients will undergo baseline and follow-up sampling of PCT. In addition, PCT should be measured if there is a clinical suspicion of infection or if antibiotic use is being considered. Where possible, antibiotic use should be commenced with appropriate support from the PCT algorithm and discontinued in compliance with repeat PCT measurement.
All care of patients with acute pancreatitis in the intervention arm will be standard with the sole exception of antibiotic use which will be guided by the PCT algorithm.

Summary methodology in the control arm:
All care of patients with acute pancreatitis in the control arm will be standard.

Duration of treatment:
Patients will remain within the study for 90 days or until discharge from hospital (if later).

Patients will be followed for 90 days or until discharge from hospital (if later).

Intervention type



Drug names

Primary outcome measures

Days of antibiotic use, defined as any day (24 hour period) when antibiotics were prescribed on the patient’s drug prescription chart and administered. This will be recorded as days of antibiotic use until the 90th day or until discharge from hospital (if later).

Secondary outcome measures

All secondary outcomes measured as occurring up to the 90th day or until discharge from hospital (if later):
1. Clinical infections as defined according to the centers for disease control
2. New isolates of multi-resistant bacteria (Clostridium difficle, vancomycin resistant enterococcus [VRE], methicillin resistant staphylococcus aureus [MRSA], carbapenemase producing enterobacteriaceae [CPE])
3. Incidence of multi-resistant organism bacteraemia
4. Infection of pancreatic necrosis, defined either as a result of fine needle aspiration (FNA), radiological evidence of gas in a peri-pancreatic collection or positive microbiological cultures from surgical or post-mortem specimens
5. Use of radiological, endoscopic or surgical intervention
6. Length of inpatient stay (by level of care: critical care levels II/III, ward-based care)
7. Re-admission to hospital within 6 weeks of onset of index episode
8. Episode-related mortality and cause
9. Quality of life, assessed by the EQ-5D-5L questionnaire
10. Cost analysis from an NHS perspective, including inpatient resource use

Overall trial start date


Overall trial end date


Reason abandoned


Participant inclusion criteria

Adult patients presenting with acute pancreatitis admitted or referred to the service. Inclusion criteria include:
1. Patients over the age of 18 years of age
2. Ability to provide informed consent
3. The diagnosis of acute pancreatitis requires two of the following three features:
3.1. Abdominal pain consistent with acute pancreatitis (acute onset of a persistent, severe, epigastric pain often radiating to the back)
3.2. Serum lipase activity (or amylase activity) at least three times greater than the upper limit of normal
3.3. Characteristic findings of acute pancreatitis on contrast-enhanced computed tomography (CECT) and less commonly magnetic resonance imaging (MRI) or transabdominal ultrasonography

Participant type


Age group




Target number of participants


Participant exclusion criteria

1. Patients under the age of 18 years of age
2. Patients who are unable to give informed consent
3. Infectious conditions requiring prolonged antibiotic therapy – such as infective endocarditis
4. Severely immunocompromised patients – such as those with human immunodeficiency virus and with a CD4 count of less than 200 cells/mm3; neutropenic patients (<500 neutrophils/mm3)
5. Patients on immunosuppressive therapy
6. Previous thyroid surgery

Recruitment start date


Recruitment end date



Countries of recruitment

United Kingdom

Trial participating centre

Manchester Royal Infirmary
Oxford Road
M13 9WL
United Kingdom

Sponsor information


Manchester University NHS Foundation Trust

Sponsor details

Oxford Road
M13 9WL
United Kingdom
+44 (0)161 276 1234

Sponsor type

Hospital/treatment centre



Funder type

Hospital/treatment centre

Funder name

Manchester University NHS Foundation Trust

Alternative name(s)

Funding Body Type

Funding Body Subtype


Results and Publications

Publication and dissemination plan

It is the trialists' intention to publish the protocol in a peer-reviewed journal. It has not currently been submitted. Clinical and economic analysis will be conducted to a prospective analysis plan made available to journal referees. The results will be presented at appropriate national and international meetings. The results will be published regardless of the final results of the trial.

IPD sharing statement
The participant-level data that will be recorded for this study are highly specific to the PROCAP analysis and should not be used for unspecified secondary analyses. Therefore the trialists do not plan to make these data available. The primary data will be stored as paper-based case report forms in a locked office in the Manchester Royal Infirmary.

Intention to publish date


Participant level data

Not expected to be available

Results - basic reporting

Publication summary

Publication citations

Additional files

Editorial Notes