Teicoplanin in Treating Septicemia in Patients Who Are Receiving Chemotherapy Through a Central Venous Catheter
Launched by CHILDREN'S CANCER AND LEUKAEMIA GROUP · Jan 26, 2003
Trial Information
Current as of May 22, 2025
Unknown status
Keywords
ClinConnect Summary
OBJECTIVES:
* Compare the response and cure rate of coagulase-negative staphylococcal septicemia in patients receiving chemotherapy through a central venous catheter treated with 2 different schedules of teicoplanin.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center and number of central venous catheter lumens (1 vs 2). Patients are randomized to one of two treatment arms.
* Arm I: Patients receive teicoplanin IV bolus every 12 hours for 3 doses and then once daily for 5 doses (total of 7 days).
* Arm II: Patients receive teicopla...
Gender
ALL
Eligibility criteria
- DISEASE CHARACTERISTICS:
- • Suspected septicemia caused by coagulase-negative staphylococci
- • Single or double lumen (no triple lumen) central venous catheter (CVC) (including subcutaneous ports) that can be flushed and aspirated
- • Expected to remain in situ for at least 8 weeks
- • No coagulase-negative septicemia associated with existing CVC within the past 12 weeks
- • Receiving chemotherapy for neoplastic condition, aplastic anemia, Fanconi's anemia, Langerhans' cell histiocytosis, or myelodysplasia
- PATIENT CHARACTERISTICS:
- Age:
- • 2 months and over
- Performance status:
- • Not specified
- Life expectancy:
- • Not specified
- Hematopoietic:
- • Not specified
- Hepatic:
- • Not specified
- Renal:
- • Creatinine clearance at least 60 mL/min
- PRIOR CONCURRENT THERAPY:
- • Biologic therapy
- • Not specified
- • Chemotherapy
- • See Disease Characteristics
- • Endocrine therapy
- • Not specified
- • Radiotherapy
- • Not specified
- • Surgery
- • Not specified
About Children's Cancer And Leukaemia Group
The Children's Cancer and Leukaemia Group (CCLG) is a leading organization dedicated to improving outcomes for children and young people diagnosed with cancer and leukaemia. Comprising a network of healthcare professionals, researchers, and patient advocates, CCLG focuses on fostering collaboration and innovation in clinical research. The group is committed to developing and implementing clinical trials that advance treatment options, enhance patient care, and ultimately provide hope for families facing these challenging diagnoses. By prioritizing evidence-based practices and patient-centered approaches, CCLG aims to drive progress in pediatric oncology and improve survival rates and quality of life for affected children.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Southampton, England, United Kingdom
Aberdeen, Scotland, United Kingdom
Leicester, England, United Kingdom
Sheffield, England, United Kingdom
Nottingham, England, United Kingdom
Edinburgh, Scotland, United Kingdom
Oxford, England, United Kingdom
London, England, United Kingdom
Belfast, Northern Ireland, United Kingdom
Dublin, , Ireland
Bristol, England, United Kingdom
Cambridge, England, United Kingdom
Liverpool, England, United Kingdom
London, England, United Kingdom
London, England, United Kingdom
Sutton, England, United Kingdom
Glasgow, Scotland, United Kingdom
Leeds, England, United Kingdom
Newcastle Upon Tyne, England, United Kingdom
Birmingham, England, United Kingdom
Manchester, England, United Kingdom
Patients applied
Trial Officials
Barry Pizer, MD
Study Chair
Royal Liverpool Children's Hospital, Alder Hey
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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