Registry of Patients With Brain Tumors Treated With STaRT (GammaTiles) (NCT04427384)
A Multicenter Observational Study of GammaTileβ’ Surgically Targeted Radiation Therapy (STaRT) in Intracranial Brain Neoplasms
π©Ί Plain-English Summary (8th-Grade Level)
The objectives of this registry study are to evaluate real-world clinical outcomes and patient reported outcomes that measure the effectiveness and safety of STaRT.
Who can join: Review the eligibility criteria below.
Location: HonorHeath Scottsdale Osborn Medical Center β Phoenix, Arizona
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π All Participating Trial Locations (54 Sites)
Showing the first 25 of 54 sites.
- HonorHeath Scottsdale Osborn Medical Center β Phoenix, Arizona
- University of Arkansas Medical Center β Little Rock, Arkansas
- Eden Medical Center β Castro Valley, California
- UCSD Moores Cancer Center β La Jolla, California
- MemorialCare Health System β Laguna Hills, California
- Desert Regional Medical Center β Palm Springs, California
- California Pacific Medical Center, Sutter health β San Francisco, California
- Centura β Denver, Colorado
- Colorado Brain & Spine Institute: Swedish Campus β Englewood, Colorado
- BayCare Health β Clearwater, Florida
- Ascension St. Vincent's β Jacksonville, Florida
- Miami Cancer Institute, Baptist Health South Florida β Miami, Florida
- Advent Health Orlando β Orlando, Florida
- Orlando Health β Orlando, Florida
- Florida Health Sciences Center, Inc. d/b/a Tampa General Hospital β Tampa, Florida
- Cleveland Clinic Florida- Weston β Weston, Florida
- Piedmont Healthcare β Atlanta, Georgia
- Winship Cancer Institute of Emory University β Atlanta, Georgia
- St. Alphonsus Regional Medical Center β Boise, Idaho
- Goodman Campbell Brain and Spine β Carmel, Indiana
- Indiana University, IU Health Methodist Hospital β Indianapolis, Indiana
- KUMC Dept of Neurosurgery β Kansas City, Kansas
- Univeristy of Louisville Health β Louisville, Kentucky
- Norton Cancer Institute β Louisville, Kentucky
- Willis-Knighton Medical Center β Shreveport, Louisiana
π Contact the Study Coordinator
Phone: (833) 662-0044
Email: mgarcia@gtmedtech.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
π° Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.