Micafungin Lock Therapy
Primary Purpose
Catheter-Related Fungal Infections
Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Micafungin lock therapy
Sponsored by
About this trial
This is an interventional treatment trial for Catheter-Related Fungal Infections focused on measuring catheter fungal infections, antimicrobial lock therapy, micafungin, central venous catheter
Eligibility Criteria
Inclusion Criteria:
- Children, 6 months-18 yrs, with a central line fungal infection, presumed Candida, admitted at Children's Medical Center.
- Signed informed consent by parents and assent by minor if applicable.
- Subjects with likely survival beyond 1 week.
Exclusion Criteria:
- Pocket, tunnel or exit-site infection
- Known allergic reactions to the Micafungin or echinocandins.
- Severe systemic symptoms (disseminated candidemia, fungal balls, endocarditis)
- Mixed infections
- Inability to lock the catheter lumen for minimum 8h because of other medications administration
- Subjects requiring ECMO or CVVH.
- Patients with HIV, congenital immunodeficiencies.
- Positive pregnancy test or breastfeeding.
Sites / Locations
- Children's Medical Center of Dallas/University of Texas Southwestern Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
1
2
Arm Description
ALT with placebo with systemic Micafungin therapy
ALT with Micafungin and heparin with systemic Micafungin therapy
Outcomes
Primary Outcome Measures
Central vascular catheter preserved during lock therapy as a result of resolution of symptoms and negative cultures within 96h.
Secondary Outcome Measures
Descriptive analysis of safety profile of patients receiving ALT and systemic micafungin
Full Information
NCT ID
NCT00809887
First Posted
December 15, 2008
Last Updated
December 15, 2008
Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
1. Study Identification
Unique Protocol Identification Number
NCT00809887
Brief Title
Micafungin Lock Therapy
Official Title
Micafungin Lock Therapy to Clear Fungemia While Attempting to Preserve Central Venous Catheters
Study Type
Interventional
2. Study Status
Record Verification Date
November 2008
Overall Recruitment Status
Terminated
Why Stopped
Inability to enroll subjects
Study Start Date
June 2006 (undefined)
Primary Completion Date
June 2008 (Anticipated)
Study Completion Date
November 2008 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study proposes to investigate, in children admitted at Children's Medical Center at Dallas, the effectiveness of antimicrobial lock therapy (ALT) with Micafungin in combination with systemic antifungal therapy in catheter-related fungal infections in order to salvage highly needed central venous catheter (CVC) and at the same time to investigate the effectiveness of Micafungin alone as systemic therapy in the treatment of Candidemia in a pediatric population.
Detailed Description
The antimicrobial lock therapy (ALT) consists of filling a catheter lumen with a supraphysiologic concentration (100- to 1000- fold higher) of an antimicrobial agent and allowing it to dwell (lock) for several hours in an attempt to sterilize the lumen. Advantages of the ALT are: the ability to administer high local concentrations; the ease of administration; the cost-savings and vein access-savings by decreasing the number of surgical procedures in an operating room for catheter replacement; the decrease in possible surgical complications and risks. The Infectious Diseases Society of America, the Society for Healthcare Epidemiology of America and others recommend the ALT for the treatment of uncomplicated bacteremias. This technique however is not currently recommended for the treatment of catheter-related fungal infections, primarily due to lack of adequate data. This study plans to enroll approximately 20 children admitted to the Children's Medical Center at Dallas in high need of central venous catheters or with evidence of fungemia in this study to investigate the effectiveness of ALT with Micafungin against fungal infections.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Catheter-Related Fungal Infections
Keywords
catheter fungal infections, antimicrobial lock therapy, micafungin, central venous catheter
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Placebo Comparator
Arm Description
ALT with placebo with systemic Micafungin therapy
Arm Title
2
Arm Type
Experimental
Arm Description
ALT with Micafungin and heparin with systemic Micafungin therapy
Intervention Type
Drug
Intervention Name(s)
Micafungin lock therapy
Primary Outcome Measure Information:
Title
Central vascular catheter preserved during lock therapy as a result of resolution of symptoms and negative cultures within 96h.
Time Frame
96 hours
Secondary Outcome Measure Information:
Title
Descriptive analysis of safety profile of patients receiving ALT and systemic micafungin
Time Frame
Up to one month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Children, 6 months-18 yrs, with a central line fungal infection, presumed Candida, admitted at Children's Medical Center.
Signed informed consent by parents and assent by minor if applicable.
Subjects with likely survival beyond 1 week.
Exclusion Criteria:
Pocket, tunnel or exit-site infection
Known allergic reactions to the Micafungin or echinocandins.
Severe systemic symptoms (disseminated candidemia, fungal balls, endocarditis)
Mixed infections
Inability to lock the catheter lumen for minimum 8h because of other medications administration
Subjects requiring ECMO or CVVH.
Patients with HIV, congenital immunodeficiencies.
Positive pregnancy test or breastfeeding.
Facility Information:
Facility Name
Children's Medical Center of Dallas/University of Texas Southwestern Medical Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
12. IPD Sharing Statement
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Micafungin Lock Therapy
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