ClinicalTrials.gov record
Terminated Phase 2 Interventional

Carboplatin as a Radiosensitizer in Treating Childhood Ependymoma

ClinicalTrials.gov ID: NCT01088035

Public ClinicalTrials.gov record NCT01088035. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 6, 2026, 8:40 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Multi-Institutional Trial of Focal Radiotherapy With Concomitant Carboplatin as a Radiosensitizer and the Prospective Analysis of Survivin, an Inhibitor of Apoptosis, as a Biomarker in Children With Newly Diagnosed Non-Metastatic Ependymoma and Minimal Residual Disease Post-Operatively

Study identification

NCT ID
NCT01088035
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Other
Enrollment
75 participants

Conditions and interventions

Conditions

Interventions

  • Carboplatin Drug

Drug

Eligibility (public fields only)

Age range
12 Months to 21 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2010
Primary completion
Dec 31, 2014
Completion
Mar 31, 2015
Last update posted
Mar 1, 2015

2010 – 2015

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Children's Memorial Hospital Chicago Illinois 60614

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01088035, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 1, 2015 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01088035 live on ClinicalTrials.gov.

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