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Spots Global Cancer Trial Database for Laser Ablation After Stereotactic Radiosurgery

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Laser Ablation After Stereotactic Radiosurgery

Official Title: Laser Ablation After Stereotactic Radiosurgery

Study ID: NCT01651078

Interventions

Study Description

Brief Summary: The need for new technologies and devices in the field of neurosurgery is well established. In April 2013, FDA cleared NeuroBlate™ System, minimally invasive robotic laser thermotherapy tool. It employs a pulsed surgical laser to deliver targeted energy to abnormal brain tissue caused by tumors and lesions. This post-marketing, multi-center study will include patients with metastatic tumors who failed stereotactic radiosurgery and are already scheduled for NeuroBlate procedure. The study will collect clinical outcome, Quality of Life (QoL) and, where feasible, healthcare utilization data for publication.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Yale School of Medicine, New Haven, Connecticut, United States

Kansas University Medical Center, Kansas City, Kansas, United States

Washington University in St Louis, Saint Louis, Missouri, United States

Carolina Neurosurgery & Spine Associates, Charlotte, North Carolina, United States

Wake Forest School of Medicine, Winston-Salem, North Carolina, United States

Cleveland Clinic, Cleveland, Ohio, United States

Thomas Jefferson University, Philadelphia, Pennsylvania, United States

Contact Details

Name: Veronica Chiang, MD

Affiliation: Yale School of Medicine

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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