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NCT00185666 · ClinicalTrials.gov registry record · Phase 1

Cyberknife Precision Radiation Delivery System for Tumors of the Spine

A Phase 1 study of Spinal Cord Cancer and Brain (Nervous System) Cancers, sponsored by Stanford University.

Completed
Registry status
Phase 1
Development phase
200
Enrollment target
1
Study location

NCT00185666: Completed Phase 1 study of Spinal Cord Cancer and Brain (Nervous System) Cancers, sponsored by Stanford University.

NCT00185666 is a Phase 1 study of Spinal Cord Cancer and Brain (Nervous System) Cancers that has completed, run by Stanford University. The registered enrollment target is 200 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (233% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00185666, a Phase 1 study of Spinal Cord Cancer and Brain (Nervous System) Cancers, has completed, sponsored by Stanford University.

COMPLETED
Registry status
Phase 1
Development phase
200 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine the usefulness of Cyberknife precision radiation in eliminating or preventing the further growth of spinal tumors and lesions.

Interventions

  • PROCEDURE Stereotactic radiosurgery

Study Locations (1)

California

  • Stanford University School of Medicine - Stanford

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2002-05
Est. Completion 2006-05
Phase Phase 1
Stanford University

1,744 total trials

What the finished NCT00185666 record still lists

NCT00185666 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (233% higher).

The record links to 2 conditions, with Spinal Cord Cancer appearing as the primary indexed condition, and to 1 intervention - of which Stereotactic radiosurgery is the first listed.

NCT00185666 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT00185666 about?

NCT00185666 is a clinical study titled "Cyberknife Precision Radiation Delivery System for Tumors of the Spine". The purpose of this study is to determine the usefulness of Cyberknife precision radiation in eliminating or preventing the further growth of spinal tumors and lesions.

What is the current status of trial NCT00185666?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 200 participants. The study started on 2002-05. Estimated completion is 2006-05.

What conditions does trial NCT00185666 study?

This clinical trial studies the following conditions: Spinal Cord Cancer, Brain (Nervous System) Cancers.

What interventions are being tested in trial NCT00185666?

The interventions under investigation include: Stereotactic radiosurgery (PROCEDURE).

Who is sponsoring clinical trial NCT00185666?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00185666 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT00185666's enrollment target sits among peer trials

200 259th of 2000 higher than 1,724 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00185666, the US trial registry maintained by the National Library of Medicine. NCT00185666 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.