Probiotics for Reduction of Infections With Clostridium Difficile in Critically Ill Patients (ProbiEnt)
Primary Purpose
Clostridium Difficile Colonisation, Impact of Enteral Probiotics on Certain Lab Parameters
Status
Terminated
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
L. plantarum 299 and L. plantarum 299v (+maltodextrin)
Maltodextrin
Sponsored by
About this trial
This is an interventional prevention trial for Clostridium Difficile Colonisation focused on measuring Clostridium difficile, WBC, CRP, Lactate, Urea, Creatinine
Eligibility Criteria
Inclusion Criteria:
- Anticipated need for intensive care 3 days or longer
- Patients condition allowing enteral nutrition to be started within 24 h from ICU admission
- Antibiotics on-going or planned
Exclusion Criteria:
- Known positive test for Clostridium difficile within the last week
- Known ulcers in the mouth, oropharynx, esophagus and stomach
- Known immune deficiencies
- Enteral nutrition contra indicated
- Pancreatitis as admission diagnosis at the hospital or at the ICU
- ICU admission earlier during this period of illness Patient being moribund
Sites / Locations
- Intensive Care Unit, Helsingborg Hospital
- Intensive Care Unit, Kristianstad Central hospital
- Lund University Hospital
- Dept of Anesthesia & Intensive Care, University Hospital of Norrland
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Probiotics
Control
Arm Description
Patients will be given a mixture of maltodextrin ( a starch product often used i alimentary products) and two strains of probiotic bacteria ( L. plantarum 299 and L. plantarum 299v ) dissolved in water through a nasogastric tube. Patients randomized 1:1 between groups
Patients will be given only the dissolved maltodextrin in water through the nasogastric tube. Patients randomized 1:1 between groups
Outcomes
Primary Outcome Measures
Differences in emerging cases of Clostridium difficile
Emerging cases of Clostridium difficile, identified as positive cultures and/or toxin tests
Secondary Outcome Measures
White blood cells
Samples taken at admission or inclusion and then daily
C Reactive Protein
Samples taken at admission or inclusion and then daily
Creatinine
Samples taken at admission or inclusion and then daily
Urea
Samples taken at admission or inclusion and then daily
Lactate
Samples taken at admission or inclusion and then daily
Ventilator days
Records are held for how long the patients require mechanical ventilation
Length of stay ICU
Length of stay is recorded for the ICU as well as for the Hospital stay
Length of Hospital stay
Length of stay is recorded for the Hospital as well as for the ICU stay
Survival
For participating patients the status of survival or non survival at days 28 and 180 (six months) will be recorded
Diarrhea and obstipation
As ICU patients tend to display diarrhea as well as obstipation the frequency and consistency of stools will be recorded.
Probiotics are anticipated to stabilise bowel function
Full Information
NCT ID
NCT01687543
First Posted
August 28, 2012
Last Updated
October 3, 2017
Sponsor
Region Skane
Collaborators
Lund University
1. Study Identification
Unique Protocol Identification Number
NCT01687543
Brief Title
Probiotics for Reduction of Infections With Clostridium Difficile in Critically Ill Patients
Acronym
ProbiEnt
Official Title
Probiotics for Reduction of Colonisation With Clostridium Difficile in Antibiotic Treated Intensive Care Patients
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Terminated
Why Stopped
Too low inclusion rate and several sites did not comply
Study Start Date
June 2012 (undefined)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
October 1, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Region Skane
Collaborators
Lund University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Symptoms of Clostridium difficile infection is almost always induced as a complication to the use of antibiotics. Most ICU patients are given antibiotics.
Probiotics has the ability to improve conditions in the gut and it has been shown in some smaller studies that overgrowth of C. difficile can be reduced or prevented.
In this study the intention is to show with sufficient statistical power that a mixture of two otherwise well studied probiotic strains reduces or prevents the incidence of emerging colonisation with C. difficile in critical ill patients on antibiotics.
Half of the patients will be given a mixture of Lactobacillus plantarum 299 and Lactobacillus plantarum 299v twice daily and the rest a placebo mixture.
Rectal swabs or faeces will be analysed for C.difficile and its toxins and the incidence of new cases will be compared for the two groups.
White blood cells (WBC´s), C reactive protein (CRP), lactate, urea, and creatinine will be followed daily as well as antibiotics, corticosteroids and all acid reducing medication.
Nutrition, enteral and total, and bowel habits will be recorded.
Detailed Description
Infections with Clostridium difficile is considered to be the most frequent health care associated bacterial infection. Almost all cases are connected to the use of antibiotics.
The spectra of symptoms of infection reaches from loose stools to sepsis and death. It is estimated that about 5% of the population are carriers without symptoms.
Elderly people are more likely to be diagnosed with C. difficile infections and as about 50 % of ICU admissions (at least in Sweden) are patients aged 64 years or older C. difficile is also an ICU issue.
Probiotic bacteria given to antibiotic treated patients results in fever cases of infection with C. difficile as we and others have shown in some small studies. Due to a low statistical power in our former study this multicentre study is calculated to be large enough to fulfil statistical requirements.
Adult patients with an expected length of stay in intensive care for three days or more can be included.
Primary objective is to find emerging cases of colonisation with C. difficile and consequent symptoms of infection such as diarrhoea.
Cultures and toxin analyses will be taken at inclusion and every second day till day 13 and then every third or fourth day depending on length of ICU stay. Positive cases will be given antibiotics according to normal routines.
No other cultures are collected per protocol but all cultures will be recorded and results will be analysed in order to find any connection between treatment and reduction of secondary infections.
In our earlier small study we found an improved and normalised gut barrier function for those patients that were given probiotic bacteria compared to a worsened, scattered pattern for the placebo group. This is probably why we found that inflammatory parameters improved for the probiotics group while those parameters remained elevated for the control patients. The same goes for creatinine, urea and lactate. This is why we will record those parameters together with blood gas analyses in this expanded study.
Antibiotics and medication with corticosteroids, proton pump inhibitors or other acid reducing preparations, All nutritive prescriptions (enteral formulas and IV solutions as well as medical preparations containing glucose or fat) will be recorded and compared to actually given nutrients.
Bowel movements frequency and consistency will be recorded and compared between groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clostridium Difficile Colonisation, Impact of Enteral Probiotics on Certain Lab Parameters
Keywords
Clostridium difficile, WBC, CRP, Lactate, Urea, Creatinine
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
25 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Probiotics
Arm Type
Experimental
Arm Description
Patients will be given a mixture of maltodextrin ( a starch product often used i alimentary products) and two strains of probiotic bacteria ( L. plantarum 299 and L. plantarum 299v ) dissolved in water through a nasogastric tube. Patients randomized 1:1 between groups
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Patients will be given only the dissolved maltodextrin in water through the nasogastric tube. Patients randomized 1:1 between groups
Intervention Type
Dietary Supplement
Intervention Name(s)
L. plantarum 299 and L. plantarum 299v (+maltodextrin)
Other Intervention Name(s)
Lactobacillus plantarum 299, Lactobacillus plantarum 299v, Maltodextrin
Intervention Description
A suspension of Lactobacillus plantarum 299 and Lactobacillus plantarum 299v together with maltodextrin is distributed to the patients twice a day.
Intervention Type
Other
Intervention Name(s)
Maltodextrin
Intervention Description
A suspension of maltodextrin (as placebo control) is distributed to the patients twice a day.
Primary Outcome Measure Information:
Title
Differences in emerging cases of Clostridium difficile
Description
Emerging cases of Clostridium difficile, identified as positive cultures and/or toxin tests
Time Frame
Throughout the ICU stay, expected mean LOS 10 days
Secondary Outcome Measure Information:
Title
White blood cells
Description
Samples taken at admission or inclusion and then daily
Time Frame
Throughout the ICU , expected mean LOS 10 days
Title
C Reactive Protein
Description
Samples taken at admission or inclusion and then daily
Time Frame
Throughout the ICU , expected mean LOS 10 days
Title
Creatinine
Description
Samples taken at admission or inclusion and then daily
Time Frame
Throughout the ICU , expected mean LOS 10 days
Title
Urea
Description
Samples taken at admission or inclusion and then daily
Time Frame
Throughout the ICU , expected mean LOS 10 days
Title
Lactate
Description
Samples taken at admission or inclusion and then daily
Time Frame
Throughout the ICU , expected mean LOS 10 days
Title
Ventilator days
Description
Records are held for how long the patients require mechanical ventilation
Time Frame
Throughout the ICU stay, expected mean LOS 10 days
Title
Length of stay ICU
Description
Length of stay is recorded for the ICU as well as for the Hospital stay
Time Frame
Length of ICU stay, about 10 days in accordance with a prior similar study
Title
Length of Hospital stay
Description
Length of stay is recorded for the Hospital as well as for the ICU stay
Time Frame
Within six months from date of ICU admission
Title
Survival
Description
For participating patients the status of survival or non survival at days 28 and 180 (six months) will be recorded
Time Frame
Six months
Title
Diarrhea and obstipation
Description
As ICU patients tend to display diarrhea as well as obstipation the frequency and consistency of stools will be recorded.
Probiotics are anticipated to stabilise bowel function
Time Frame
Throughout the ICU stay, expected mean LOS 10 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Anticipated need for intensive care 3 days or longer
Patients condition allowing enteral nutrition to be started within 24 h from ICU admission
Antibiotics on-going or planned
Exclusion Criteria:
Known positive test for Clostridium difficile within the last week
Known ulcers in the mouth, oropharynx, esophagus and stomach
Known immune deficiencies
Enteral nutrition contra indicated
Pancreatitis as admission diagnosis at the hospital or at the ICU
ICU admission earlier during this period of illness Patient being moribund
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bengt Klarin, MD, PhD
Organizational Affiliation
Lund University, Lund, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Intensive Care Unit, Helsingborg Hospital
City
Helsingborg
ZIP/Postal Code
SE 251 87
Country
Sweden
Facility Name
Intensive Care Unit, Kristianstad Central hospital
City
Kristianstad
ZIP/Postal Code
SE 291 85
Country
Sweden
Facility Name
Lund University Hospital
City
Lund
ZIP/Postal Code
SE 22185
Country
Sweden
Facility Name
Dept of Anesthesia & Intensive Care, University Hospital of Norrland
City
Umeå
ZIP/Postal Code
SE-901 85
Country
Sweden
12. IPD Sharing Statement
Citations:
PubMed Identifier
18840110
Citation
Klarin B, Wullt M, Palmquist I, Molin G, Larsson A, Jeppsson B. Lactobacillus plantarum 299v reduces colonisation of Clostridium difficile in critically ill patients treated with antibiotics. Acta Anaesthesiol Scand. 2008 Sep;52(8):1096-102. doi: 10.1111/j.1399-6576.2008.01748.x.
Results Reference
background
Links:
URL
http://www.probi.se
Description
Producers of the study products
Learn more about this trial
Probiotics for Reduction of Infections With Clostridium Difficile in Critically Ill Patients
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