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One-Time zap: new radiation approach aims to ease spine tumor pain

NCT ID NCT00492817

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a single, precise session of high-dose radiation (stereotactic body radiotherapy) can safely relieve pain and control tumor growth in people with cancer that has spread to the spine. 71 adults with up to two spine tumors participated. Researchers measured pain relief, tumor control, and any nerve damage over 6 months.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1/2

Runs two stages together: safety and dose first, then whether the treatment works.

Participants

71 people

The number who actually took part.

Started

Oct 2005

Finished

Nov 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Radiographically documented spine or paraspinal metastasis demonstrated on spine MRI within 4 weeks of registration 2. Maximum of 2 metastatic sites in the spine to be irradiated in single session 3. Informed consent for irradiation of spinal or para-spinal tumor (s) 4. Diagnosis of cancer including but not limited to lung (non-small cell and small cell), breast, prostate, renal cell, melanoma, gastrointestinal, and germ cell tumors, unknown primary tumors 5. Karnofsky performance status of at least 40 (ie not requiring active hospitalization) Exclusion Criteria: 1. Worsening neurological status due to radiographic evidence of spinal cord compression requiring immediate surgical decompression or emergent conventional external radiation therapy. 2. Delay in initiation of radiation treatment would be potentially detrimental to neurological outcome 3. Prior irradiation to current site of interest in the spine 4. Spinal metastasis in the cervical spine are not eligible for treatment 5. Unstable spine requiring surgical stabilization. 6. Sites outside the spine (eg. lung, liver) are not eligible for treatment 7. Patients currently receiving, or who have received chemotherapy within 30 days are not eligible 8. Inability to tolerate lying flat on treatment couch for greater than 30 minutes. 9. Patient with multiple myeloma 10. Patients unable to undergo MRI of the spine 11. Patients with pacemakers

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Conditions

The condition(s) this trial relates to.

spinal cord neoplasm Spinal Neoplasms

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • University of Texas MD Anderson Cancer Center

    Houston, Texas, 77030, United States

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Other studies related to the condition(s) this trial covers.