- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00798330
Dental Study in Cancer Patients With Central Venous Catheters
August 25, 2020 updated by: Rajesh Lalla
Pilot Study on Transient Bacteremia and Blood Stream Infections After Invasive Dental Procedures in Cancer Patients With Central Venous Catheters
Patients who are preparing to receive chemotherapy are asked to have their teeth cleaned before starting treatment as standard of care.
This research study is being done to see if having dental cleaning increases the chances of bacteria from the mouth getting into the blood stream.
It is also being done to see if these bacteria can cause blood stream infections in people who have a Central Venous Catheter (CVC),often called a "port" or a "PICC", placed for giving chemotherapy.
It is a well-established fact that we introduce bacteria from the mouth into the bloodstream with activities of daily life including chewing, flossing and brushing teeth.
This introduction of bacteria into the blood stream may cause bacteria to stick to the central venous catheter and serve as a source of infection when the immune system is weakened by cancer.
The purpose of this research study is to see if we can find bacteria from mouth in blood that is drawn through the CVC, during, and after a dental cleaning procedure.
This way, we will be able to assess whether or not this is a potential health risk to cancer patients.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
27
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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Connecticut
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Farmington, Connecticut, United States, 06030
- University of Connecticut Health Center
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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
Cancer outpatients with central venous catheters (Medport or PICC lines)
Description
Inclusion criteria
- Patients willing and able to provide written informed consent for the study.
- Patients diagnosed with cancer and being treated at the University of Connecticut Health Center.
- Patients scheduled to receive or who have received a central venous catheter
- Patients who have at least one tooth.
Exclusion criteria
- Patients under the age of 18
- Patients who have received any antibacterial in the time period starting 48 hours before the dental cleaning. This includes systemic antibacterials and topical antibacterials in the oral cavity or at/through the CVC site. (Topical antibacterials at other sites are allowed; antifungal and antiviral agents in any form are allowed).
- Patients who plan to use antibacterials within the 24 hours after the procedure (until the final blood sample is obtained).
- Patients with a documented blood stream infection within 1 month prior to proposed dental cleaning.
- Patients with a clinically significant coagulation disorder or patients on warfarin.
- Patients who require antibiotic prophylaxis as per American College of Cardiology/American Heart Association (ACC/AHA) 2007 guidelines, namely;
- patients who have had a cardiac transplantation,
- incomplete cardiac valve repair,
- complete cardiac valve repair in last 6 months,
- prior history of infective endocarditis ,
- patients with a prosthetic cardiac valve.
- Patients with any other condition which might preclude participation in the opinion of the patient's physician(s) or the study PI's.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To determine the incidence of transient bacteremia and established blood-stream infections (BSIs) by oral microorganisms in cancer patients with CVCs after an invasive dental procedure
Time Frame: Two days, 1 month, 6 months
|
Blood cultures drawn before dental cleaning, 20 minutes after starting procedure, 30 minutes after finishing the procedure and at 24 hours after starting the procedure.
Records reviewed at one month and six months post procedure for bloodstream or central venous catheter infection.
|
Two days, 1 month, 6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Rajesh V Lalla, DDS, Ph.D, UConn Health
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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
September 1, 2012
Primary Completion (Actual)
December 1, 2012
Study Completion (Actual)
December 1, 2012
Study Registration Dates
First Submitted
November 25, 2008
First Submitted That Met QC Criteria
November 25, 2008
First Posted (Estimate)
November 26, 2008
Study Record Updates
Last Update Posted (Actual)
August 27, 2020
Last Update Submitted That Met QC Criteria
August 25, 2020
Last Verified
August 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 09-059-2
- 786-001
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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