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Completed Not applicable Interventional Results available

Stereotactic Radiation Therapy for Pediatric Sarcomas

ClinicalTrials.gov ID: NCT01763970

Public ClinicalTrials.gov record NCT01763970. 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 Sep 5, 2026, 3:17 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 Study of Hyperfractionated Stereotactic Radiotherapy in the Treatment of Metastatic Pediatric Sarcomas of Bony Sites

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The stereotactic body radiation therapy (SBRT) literature focuses on clinical outcomes in the adult population. However, SBRT has a particularly strong rationale for application in pediatrics given that high biologically effective doses have been shown to increase control in histologies, such as sarcoma, which are common in the pediatrics population. With stereotactic radiation therapy techniques, a reduction in normal tissue dose surrounding the target lesion of interest may also be accomplished resulting in lower toxicity. Given that pediatric patients with sarcomas, presenting with limited metastases in lung and bone, are still considered to be a curable population with aggressive local therapy, SBRT could have a significant impact on outcomes in oligometastatic patients who may be otherwise unresectable.

Study identification

NCT ID
NCT01763970
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
14 participants

Conditions and interventions

Interventions

Radiation

Eligibility (public fields only)

Age range
4 Years to 40 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
Oct 31, 2013
Primary completion
Sep 23, 2018
Completion
Mar 31, 2020
Last update posted
Aug 26, 2020

2013 – 2020

United States locations

U.S. sites
5
U.S. states
5
U.S. cities
5
Facility City State ZIP Site status
Stanford Medical Center Stanford California 94305-5847
Sibley Memorial Hospital Washington D.C. District of Columbia 20016
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21231
Mayo Clinic Rochester Minnesota 55902
St. Jude Children's Research Hospital Memphis Tennessee 38105-3678

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 NCT01763970, 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 Aug 26, 2020 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01763970 live on ClinicalTrials.gov.

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