Catheter-Related Infections Clinical Trial
Official title:
Treatment of Infected Dialysis Catheters With Fiber Optic Ultraviolet Light
NCT number | NCT02899780 |
Other study ID # | UVI-Pilot |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | May 11, 2017 |
Est. completion date | May 10, 2018 |
Verified date | October 2018 |
Source | Ultraviolet Interventions |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study is a first-in-man clinical trial using fiber optically delivered ultraviolet light for reducing viable bacteria within indwelling tunneled dialysis catheters.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | May 10, 2018 |
Est. primary completion date | May 10, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Be at least 18 years of age - Have the ability to provide informed consent - Have an implanted dialysis catheter of one of the following models: Medcomp Titan 15.5F x 24 cm or Medcomp Titan 15.5F x 28 cm - Positive blood culture drawn from the catheter Exclusion Criteria: - Previous inclusion in study - Pregnant |
Country | Name | City | State |
---|---|---|---|
United States | University of Maryland Medical Center | Baltimore | Maryland |
Lead Sponsor | Collaborator |
---|---|
Ultraviolet Interventions | University of Maryland |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Quantitative reduction of bacterial counts from blood cultures drawn from the dialysis catheter | Measured immediately after UV treatment | ||
Primary | Proportion of patients with any reduction of bacterial counts from blood cultures drawn from the dialysis catheter | Measured at study end, expected at 1 year. | ||
Secondary | Number of colony forming units (CFU) per cm2 of surface area on the inner lumen of removed catheters | Measured after UV treatment, with results expected in 5 days. | ||
Secondary | Procedural complications, including excessive bleeding, infection, vascular injury, and significant catheter damage. | Measured at study end, expected at 1 year. |
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