Frontlight ResearchEarly access
Not yet taking people in NorwayPhase 2
Measuring Brain Fluid Clearance to Tailor Spinal Chemotherapy in Teens With Leukemia or Lymphoma
Estimates brain fluid clearance in teens receiving chemotherapy into the spinal fluid.
Key facts
- Who runs it
- Oslo University Hospital HF
- Where
- Oslo, NorwaySee the site
- Trial code
- Registry title
- Individualized Intrathecal Chemotherapy Based on Measurement of Brain Fluid Clearance in Pediatric Patients
- Status
- Not yet recruiting
- Phase
- Phase 2
- People taking part
- 50 people, planned
- Started
- 1 Sept 2026
- Expected to end
- 31 Dec 2033
- Type of study
- Interventional
- Record updated
- 4 August 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for children aged 12 to 17 years with blood or lymph cancer who are already having intrathecal chemotherapy with MTX at Oslo University Hospital.
- Age
- 12 to 17 years
- Sex
- Both male and female can join.
- Disease stage
- Blood or lymph cancer treated with intrathecal chemotherapy with MTX.
- Earlier treatment
- Must be undergoing intrathecal chemotherapy with MTX for blood or lymph cancer.
Main reasons for not taking part
- Renal failure
- Allergy to contrast agents
- Lowered seizure threshold
- Pregnancy or breast feeding
- Body weight not above 50 kg (110 lb)
The registry criteria, word for word
Show all 9 criteriaShow less
Who can take part
- Age. Participant must be in the age range 12 to 17 years at the time of signing the informed consent
- Type of Participant and Disease Characteristics. Individuals undergoing intrathecal chemotherapy with MTX for blood or lymph cancer and being treated at Oslo University Hospital
- Weight. Body weight is above 50 kg
- Sex and Contraceptive/Barrier Requirements. Both male and female. WOCBP may be included only if they meet protocol pregnancy-testing requirements, have a confirmed menstrual period, have a negative highly sensitive urine or serum pregnancy test before inclusion/intervention, and use highly effective contraception where applicable from inclusion through Day 7 safety follow-up. WOCBP means a post-menarche female participant who is not permanently sterile and not post-menopausal
- Informed Consent. Documented informed consent/assent must be obtained before any study-specific procedure. Ages 12-15: consent from person(s) with parental responsibility plus age-adapted information and assent/participation according to maturity. Ages 16-17: participant informed consent plus consent from person(s) with parental responsibility. If a participant reaches 18 years before further protocol-defined procedures, express adult informed consent must be obtained
Who cannot take part
- Medical condition. Renal failure
- Medical condition. Hypersensitivity/Allergy to contrast agents
- Medical condition. Lowered seizure threshold
- Other. Pregnancy or breast feeding
Where in Norway
- Oslo University Hospital HFOslo, NorwayNot yet recruiting
About the trial
What the trial wants to find out
Investigate/estimate brain fluid clearance (BFC) at the individual level in children aged 12-17 years undergoing clinically indicated intrathecal chemotherapy (methotrexate, and where applicable cytarabine) for blood or lymph cancer.
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record
Print a page for my doctorData and sources
- Registry record
- Listed on the EU's official list of trials (CTIS).
- Official title
- Individualized Intrathecal Chemotherapy Based on Measurement of Brain Fluid Clearance in Pediatric Patients
- Plain-language title
- Measuring Brain Fluid Clearance to Tailor Spinal Chemotherapy in Teens With Leukemia or LymphomaGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 9 November 2026.
- Record updated
- 4 August 2026