CiproPAL (Ciprofloxacin Prophylaxis in Acute Leukaemia)
Launched by UNIVERSITY COLLEGE, LONDON · Dec 16, 2020
Trial Information
Current as of July 12, 2025
Recruiting
Keywords
ClinConnect Summary
The CiproPAL trial is a study looking at whether taking a daily antibiotic called ciprofloxacin can help prevent infections in children who are starting treatment for Acute Lymphoblastic Leukaemia (ALL). This trial is part of a larger study called ALLTogether-1 and aims to see if ciprofloxacin can reduce the number of infections during the first phase of treatment, as well as to understand how it affects the development of antibiotic resistance in bacteria.
To be eligible for this study, children aged between 1 and 17 years who are newly diagnosed with ALL and are beginning their treatment in the UK within the first two weeks can participate, as long as their parent or guardian gives written consent. Participants will be randomly assigned to either receive ciprofloxacin or the usual local care they would typically get. It's important to note that certain children, such as those with specific health conditions or those already on ciprofloxacin, cannot join. This trial is currently open for recruitment, and it aims to provide valuable information on how to better protect young patients from infections during their treatment.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Paediatric patients (1-17 years inclusive) with de-novo Acute Lymphoblastic Leukaemia treated on ALLTogether-1 in the UK in the first 5 days of therapy, up to 14 days is acceptable.
- • Written informed consent
- Exclusion Criteria:
- • Non-participants of the ALLTogether-1 trial
- • Patients with Down syndrome who already receive ciprofloxacin prophylaxis
- • Chronic active arthritis
- • Other contraindication to fluoroquinolones
About University College, London
University College London (UCL) is a leading global research institution renowned for its commitment to advancing healthcare through innovative clinical trials. As a prominent sponsor of clinical research, UCL leverages its multidisciplinary expertise and state-of-the-art facilities to conduct rigorous investigations aimed at improving patient outcomes and addressing pressing medical challenges. The institution fosters collaboration among researchers, healthcare professionals, and industry partners, ensuring that its trials adhere to the highest ethical standards and regulatory guidelines. UCL's dedication to translating scientific discoveries into practical applications underscores its role as a vital contributor to the advancement of medical science and public health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Southampton, , United Kingdom
Manchester, , United Kingdom
Leeds, , United Kingdom
London, , United Kingdom
Sheffield, , United Kingdom
Cambridge, , United Kingdom
Leicester, , United Kingdom
Bristol, , United Kingdom
Oxford, , United Kingdom
Liverpool, , United Kingdom
Newcastle, , United Kingdom
Aberdeen, , United Kingdom
Nottingham, , United Kingdom
London, , United Kingdom
Patients applied
Trial Officials
Robert Phillips
Principal Investigator
University of York
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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