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NCT01254903 · ClinicalTrials.gov registry record · Phase 1
Phase I Study of Feasibility of Single Session Spine Stereotactic Radiosurgery (SSRS) in the Primary Management in Patients With Inoperable, Previously Unirradiated Metastatic Epidural Spinal Cord Compression (MESCC)
A Phase 1 study of Metastatic Epidural Spinal Cord Compression, sponsored by M.D. Anderson Cancer Center.
- Active
- Registry status
- Phase 1
- Development phase
- 43
- Enrollment target
- 1
- Study location
NCT01254903 is a Phase 1 study of Metastatic Epidural Spinal Cord Compression that is active but no longer recruiting, run by M.D. Anderson Cancer Center. The registered enrollment target is 43 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01254903, a Phase 1 study of Metastatic Epidural Spinal Cord Compression, is active but no longer recruiting, sponsored by M.D. Anderson Cancer Center.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 1
- Development phase
- 43 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical study is to learn the feasibility of using a single session of radiation, known as spine stereotactic radiosurgery (SSRS), to treat metastatic epidural spinal cord compression.
Conditions Studied
Interventions
- PROCEDURE Stereotactic Radiosurgery (SSRS)
Study Locations (1)
Texas
- University of Texas MD Anderson Cancer Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 43 participants |
| Start Date | 2010-12-03 |
| Est. Completion | 2027-04-01 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01254903
The ClinicalTrials.gov registry entry for NCT01254903 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Metastatic Epidural Spinal Cord Compression appearing as the primary indexed condition, and to 1 intervention - of which Stereotactic Radiosurgery (SSRS) is the first listed.
NCT01254903 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT01254903 about?
NCT01254903 is a clinical study titled "Phase I Study of Feasibility of Single Session Spine Stereotactic Radiosurgery (SSRS) in the Primary Management in Patients With Inoperable, Previously Unirradiated Metastatic Epidural Spinal Cord Compression (MESCC)". The goal of this clinical study is to learn the feasibility of using a single session of radiation, known as spine stereotactic radiosurgery (SSRS), to treat metastatic epidural spinal cord compression.
What is the current status of trial NCT01254903?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 43 participants. The study started on 2010-12-03. Estimated completion is 2027-04-01.
What conditions does trial NCT01254903 study?
This clinical trial studies the following conditions: Metastatic Epidural Spinal Cord Compression.
What interventions are being tested in trial NCT01254903?
The interventions under investigation include: Stereotactic Radiosurgery (SSRS) (PROCEDURE).
Who is sponsoring clinical trial NCT01254903?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01254903 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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