NotablePrimary completion date: Dec 2025 to Mar 2027
Study completion date: Feb 2026 to Mar 2028
v22
2 versionsRe-verified since Jan 4, 2025, no change to tracked fieldsv20-v21
NotablePrimary completion date: Dec 2023 to Dec 2025
Study completion date: Dec 2023 to Feb 2026
v19
NotablePrimary and study completion dates: Dec 2022 to Dec 2023v18
NotablePrimary completion date: Dec 2021 to Dec 2022v17
Show 15 earlier versionsHide 15 earlier versions
NotablePrimary completion date: Dec 2020 to Dec 2021
Study completion date: Dec 2020 to Dec 2022
v16
5 versionsRe-verified since Apr 3, 2015, no change to tracked fieldsv11-v15
NotablePrimary endpoint revisedv10
StoppedTrial status: Recruiting to Suspended
Primary and study completion dates: Dec 2020
Site details revised
v9
MinorSite contact updatedv8
MinorSecondary endpoints: details revised at 1 of 2 entriesv7
Re-verified, no change to tracked fieldsv6
NotablePhase: Not applicable to Not specified
Primary endpoints: 2 to 1
Secondary endpoints revised (2)
Site contact updated
v5
Re-verified, no change to tracked fieldsv4
MinorSite contact updatedv3
NotablePrimary endpoints: 3 to 2v2Show 4 more changesShow less
Secondary endpoints revised (2)
Study title expanded, about 7 words
Eligibility criteria expanded, about 4 words
Study description shortened, about 2 words
Study First Submitted
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to assess short and long term outcomes after radiofrequency ablation (RFA) of pulmonary malignancies in patients who are not candidates for surgical resection. This study will evaluate the efficacy of RFA for the treatment of lung tumors by assessing its impact on local tumor control, progression free survival, overall survival, dyspnea score and quality of life (QOL).