EUCTR2013-000052-17-GB
Active, not recruiting
Not Applicable
Pilot study to investigate the early prediction of toxicity following induction chemotherapy in Ewing’s sarcoma by blood-borne biomarkers and correlation with age-dependent pharmacokinetic variation - Pharmacokinetic variation and toxicity in Ewing's sarcoma
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Ewing sarcoma patients
- Sponsor
- The Newcastle Upon Tyne Hospitals NHS Foundation Trust
- Status
- Active, not recruiting
- Last Updated
- 11 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a) Diagnosis of histologically confirmed Ewing sarcoma.
- •b) Receiving VIDE or VDC/IE as part of standard clinical treatment.
- •c) Single or double lumen central venous catheter in place.
- •d) Written informed consent.
- •e) Protocol approval by national and local ethics committee, regulatory authority and Trust R\&D Departments.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 90
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range 30
- •F.1\.3 Elderly (\>\=65 years) no
Exclusion Criteria
- •a) Receiving non\-standard dose chemotherapy.
- •b) Glomerular filtration rate \<60 ml/min/1\.73m2\.
Outcomes
Primary Outcomes
Not specified
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