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Precision radiation may offer better pain relief for spine metastases

NCT ID NCT02800551

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 more intense, precisely targeted type of radiation (SBRT) works better than standard radiation for reducing pain from cancer that has spread to the spine. About 219 adults with painful spinal metastases took part. The main goal was to see if SBRT leads to greater pain improvement at 6 months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
radiation therapy (stereotactic body radiation therapy vs. conventional 3D conformal radiotherapy)
What this could lead to
If it works, this could provide better and longer-lasting pain relief for people with cancer that has spread to the spine, potentially improving quality of life.
What could go wrong
This is a phase 2 trial, so results are still preliminary. The higher radiation dose might also cause more side effects, and the benefit may not be large enough to change standard practice.

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 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

219 people

The number who actually took part.

Started

Jul 2016

Finished

Mar 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

18 years and older

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: * Established histological diagnosis of a malignant primary or metastatic tumor; * Histologically, radiologically or scintigraphically proven spinal metastasis; * Pain in the affected spinal region or free of pain under pain medication; * Age ≥18 years old; * Karnofsky performance status ≥60%; * Written informed consent. Exclusion Criteria: * Modified Bauer Score \< 2; * No-mass-type metastatic lesion, defined as a 3D space-occupying lesion visible on CT and/or MR; * "Radiosensitive" histology of the primary tumor, e.g., lymphoma, small-cell lung cancer, multiple myeloma, germ cell tumors; * Progressive neurological symptoms/deficit; * More than 3 affected vertebrae in one target site; * More than 2 treatment sites; * Spinal Instability Neoplastic Score (SINS) 13 - 18, i.e., unstable; * Unable to tolerate treatment (unable to lie flat and immobilized); * Previous radiotherapy of the region at the level of the affected vertebrae; * Previous radionuclide therapy within 30 days before stereotactic body radiation therapy; * Previous surgery (stabilization) of the affected vertebrae; * Contraindications for MR scanning, e.g., pacemakers; * Patients with allergy to contrast agents used in computer tomography (CT) and magnetic resonance (MR) imaging or patients who cannot be premedicated to use contrast agent; * Pregnant or lactating women; * Women of child bearing potential or sexually active males not willing to use effective contraception while on treatment and 3 months after the end of treatment; * Mental conditions rendering the patient unable to understand the nature, scope, and possible consequences of the study; * Patient unlikely to comply with protocol, i.e. uncooperative attitude, inability to return for follow-up visits, and unlikely to complete the study.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • UniversitätsSpital Zürich, Klinik für Radio-Onkologie

    Zurich, 8091, Switzerland

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