Bronchoscopic Lung Ablation of Small Thoracic Tumors: the Blastt Registry
2 other identifiers
observational
250
1 country
1
Brief Summary
To aggregate, integrate, and analyze data facilitating the study of MD Anderson patients with a known diagnosis of lung cancer or metastases to the lungs who undergo robotic assisted bronchoscopic ablation of peripheral tumors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2025
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 17, 2025
CompletedStudy Start
First participant enrolled
February 19, 2025
CompletedFirst Posted
Study publicly available on registry
February 21, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2034
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2036
December 18, 2025
December 1, 2025
9.9 years
February 17, 2025
December 10, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
To aggregate, integrate, and analyze data facilitating the study of MD Anderson patients with a known diagnosis of lung cancer or metastases to the lungs who undergo robotic assisted bronchoscopic ablation of peripheral tumors.
Through study completion, an average of 1 year.
Study Arms (1)
Small Thoracic Tumors
Eligibility Criteria
MD Anderson Cancer Center
You may qualify if:
- Patients with peripheral lung tumors (primary or metastatic) that have been or will be ablated via robotic bronchoscopy.
You may not qualify if:
- Patients with planned bronchoscopic ablations of peripheral lung tumors that were aborted for technical reasons (ablation was not completed).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
MD Anderson Cancer Center
Houston, Texas, 77030, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Roberto F Casal, MD
Prinicipal Investigator
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 17, 2025
First Posted
February 21, 2025
Study Start
February 19, 2025
Primary Completion (Estimated)
December 31, 2034
Study Completion (Estimated)
December 31, 2036
Last Updated
December 18, 2025
Record last verified: 2025-12