A Study to Determine if Antibiotics Prevent Infection in the Pancreas of Patients Where Part of the Pancreas Has Died
| Status: | Completed |
|---|---|
| Conditions: | Gastrointestinal |
| Therapuetic Areas: | Gastroenterology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 9/2/2017 |
| Start Date: | February 2003 |
| End Date: | December 2004 |
A Multicentre, Randomised, Double-blind, Placebo-controlled, Study on the Use of Prophylactic Meropenem Therapy in Subjects With Severe Acute Necrotizing Pancreatitis
This is a research study in patients having a condition known as necrotizing pancreatitis.
This is inflammation of the pancreas (an intestinal organ which assists with digestion) that
has resulted in the damage and death of some pancreatic tissue. This damaged pancreatic
tissue may develop a bacterial infection, which can cause further -sometimes very serious-
health problems.
It may be possible to prevent or delay infection by giving 'prophylactic' antibiotics (that
is - to provide protection before any infection starts). However, it is not certain that this
antibiotic therapy will be successful.
This study is being carried out to see whether the antibiotic 'Meropenem' (which is also
known as MERREM I.V.) provides protection from developing a pancreatic infection. This will
be done by comparing the progress of patients who receive meropenem with those who receive a
non-active placebo solution (a solution that does not contain any active medication).
Meropenem or placebo would be given in addition to the standard treatment received for
pancreatitis.
It is not known if meropenem will help prevent infections associated with necrotizing
pancreatitis.
Approximately 240 patients will take part in this study.
Study participation will be carried out for up to 6 weeks, and patients will receive the
study treatment up to a maximum of 21 days.
This is inflammation of the pancreas (an intestinal organ which assists with digestion) that
has resulted in the damage and death of some pancreatic tissue. This damaged pancreatic
tissue may develop a bacterial infection, which can cause further -sometimes very serious-
health problems.
It may be possible to prevent or delay infection by giving 'prophylactic' antibiotics (that
is - to provide protection before any infection starts). However, it is not certain that this
antibiotic therapy will be successful.
This study is being carried out to see whether the antibiotic 'Meropenem' (which is also
known as MERREM I.V.) provides protection from developing a pancreatic infection. This will
be done by comparing the progress of patients who receive meropenem with those who receive a
non-active placebo solution (a solution that does not contain any active medication).
Meropenem or placebo would be given in addition to the standard treatment received for
pancreatitis.
It is not known if meropenem will help prevent infections associated with necrotizing
pancreatitis.
Approximately 240 patients will take part in this study.
Study participation will be carried out for up to 6 weeks, and patients will receive the
study treatment up to a maximum of 21 days.
Inclusion Criteria:
- Diagnosis of necrotizing pancreatitis within 120 hours following onset of
symptoms/first reported symptoms.
- Primary diagnosis to be confirmed by contrast-enhanced CT evidence of 30% necrosis of
the pancreas.
- Or if > or equal to 30% necrosis is not present or cannot be confirmed, a contrast
enhanced CT scan showing extensive or multiple pancreatic fluid collections and
pancreatic edema (Balthazar Grade E) with either C-reactive protein (CRP). 120 mg/L or
a MOD score of > 2 is acceptable.
Exclusion Criteria:
- Received an investigational drug or device within 30 days prior to entering study.
- Received > 48 hours of antibiotic therapy between onset of symptoms of pancreatitis
and diagnosis of necrotizing pancreatitis.
- The subject has known or suspected anaphylactic or other type 1 (immediate)
hypersensitivity reactions to cephalosporins, penicillins or carbapenems.
- The subject is receiving, or will require, probenecid therapy.
- The subject is neutropenic (absolute neutrophil count < 1000/mm 3).
- The subject has cirrhosis, severity of Child's grade C.
- There is not a commitment on the part of the clinical care team, the subject, or the
subject's family to full, aggressive support including operative intervention if
needed.
- The subject is a pregnant and/or nursing female
We found this trial at
10
sites
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