- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01481038
Anticipative Diagnosis of Central Venous Catheter Related Bloodstream Infections
May 2, 2016 updated by: Robert Krause, MD, Medical University of Graz
Anticipative Diagnosis of Central Venous Catheter Related Bloodstream Infections Using Biphasic PNA FISH and Gram Stain/AOLC Tests
Up to date methods for diagnosis of Catheter Related Bloodstream Infections (CRBSI) are performed only when CRBSI is clinically suspected.
Thus, patients may actually suffer from CRBSI and are at risk to concurrently suffer from or develop complications like endocarditis or septic embolism when diagnostic procedures for the detection of CRBSI are introduced.
The aim of the project is to investigate a more sensitive and specific test for anticipative diagnosis of CRBSI using biphasic PNA FISH test compared to Gram stain/AOLC test.
Study Overview
Status
Completed
Detailed Description
Management of patients with hematologic malignancies, renal failure or diseases requiring intensive care often necessitates the use of central venous catheters (CVC).
Beside obvious advantages CVCs bear a great risk for local or systemic infections.
In the US estimated 250 000 catheter-related blood stream infection (CRBSIs) occur each year with mortality rates of 12-25%.
Diagnosis of CRBSIs remains challenging as systemic clinical signs are unspecific and local signs of infection are often absent.
Conventional methods for diagnosing CRBSIs require removal of the CVC.
However, only 15% of CVCs removed in patients with clinical suspicion of CRBSI prove to be infected.
It has been shown that CRBSI can also be detected by the differential time to positivity (DTP) method without catheter removal.
The Gram stain/acridine-orange leukocyte cytospin (AOLC) test and PNA FISH test are another methods for the diagnosis of CRBSI that does not require the removal of the CVC and additionally have shown to be fast.
Up to date methods for diagnosis of CRBSI are performed only when CRBSI is clinically suspected.
Thus, patients may actually suffer from CRBSI and are at risk to concurrently suffer from or develop complications like endocarditis or septic embolism when diagnostic procedures for the detection of CRBSI are introduced.
Since CRBSIs are not entirely preventable by strict hygiene measures earlier diagnosis of CRBSI in subclinical stages is desirable to avoid CRBSI-associated morbidity and mortality.
Previously a pilot study showed that Gram stain/AOLC screening of CVCs in neutropenic patients was a useful test to predict the development of CRBSI on average 48 hours before the diagnosis was established by routine measures.
In the pilot study Gram stain/AOLC screening test exhibited high specificity whereas sensitivity was moderate.
PNA FISH is a specific slide-based staining technique that provides pathogen identification from blood samples containing a given amount of bacteria or fungi within a 1,5 hours.
PNA FISH test has a slightly lower detection limit compared to Gram stain/AOLC which might therefore result in higher sensitivity when used as a screening tool.
The aim of the project is to investigate a more sensitive and specific test for anticipative diagnosis of CRBSI using biphasic PNA FISH test compared to Gram stain/AOLC test.
Study Type
Observational
Enrollment (Actual)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Stmk
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Graz, Stmk, Austria, 8036
- Medical University of Graz
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients undergoing hemodialysis using a central venous catheter and Patients with underlying hematooncologic disease with central venous catheters
Description
Inclusion Criteria:
- Patients undergoing hemodialysis using a central venous catheter and
- Patients with underlying hematooncologic disease with central venous catheters
Exclusion Criteria:
- No central venous catheter
- Current CRBSI
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Group dialysis patients
Patient on hemodialysis with central venous catheter
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Group hematology patients
Patients with hemato-oncologic underlying disease (plus/minus hematopoietic stem cell transplantation HSCT) and central venous catheter
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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development of crbsi
Time Frame: Participants will be followed for the development of CRBSI during the duration of central venous catheter usage, an expected average of 1 year in hemodialysis patients and an expected average of six weeks in HSCT patients.
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There is only one outcome measure that is evaluated in two patient cohorts.
Screening of catheter blood for microbial burden is performed during the whole study.
Outcome measure is the development of CRBSI in these screened patients.
Patients on hemodialysis using a CVC will be screened and observed for an sheduled time of approx.
1,5 years or until the CVC will be removed and hemodialysis no longer necessary.
Patients undergoing HSCT will be screened and observed until CVC will be removed.
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Participants will be followed for the development of CRBSI during the duration of central venous catheter usage, an expected average of 1 year in hemodialysis patients and an expected average of six weeks in HSCT patients.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2011
Primary Completion (Actual)
December 1, 2015
Study Completion (Actual)
May 1, 2016
Study Registration Dates
First Submitted
November 16, 2011
First Submitted That Met QC Criteria
November 28, 2011
First Posted (Estimate)
November 29, 2011
Study Record Updates
Last Update Posted (Estimate)
May 3, 2016
Last Update Submitted That Met QC Criteria
May 2, 2016
Last Verified
May 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CRBSI FFG Bridge
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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