CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 130 target
Drug / intervention
Online adaptive SBRT +1 moreradiation
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06542159
NCT06542159Phase 2RecruitingOn TrackUpdated 7mo ago

Elimination of PTV Margins Based on Online Adaptive Stereotactic Radiotherapy for Early-stage Non-small Cell Lung Cancer or Pulmonary Oligometastases: a Prospective, Randomized, Controlled Phase II Study

Sun Yat-sen University·interventional·Posted Aug 7, 2024·Updated Nov 17, 2025

In Brief

A Phase 2 clinical trial evaluating Online adaptive SBRT and Conventional SBRT for Adaptive Radiotherapy and 4 related conditions. Currently recruiting, targeting 130 participants across 1 site.

Detailed Summary

This study aims to explore the safety and efficacy of eliminating the PTV (planning target volume) margins based on online adaptive stereotactic radiotherapy for patients with early-stage non-small cell lung cancer (NSCLC) or pulmonary oligometastases.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2Recruiting
2025202620272028
First PostedAug 7, 2024
Enrollment StartMay 22, 2024
Primary CompletionApr 21, 2027
Study CompletionApr 21, 2028
TodayJul 1, 2026
Enrollment to primary: 2.9 yearsPosted 1.9 years agoPrimary completion in 10 months

Interventions

Online adaptive SBRTradiation

Online adaptive SBRT (without PTV expansion margin). The total dose will be 45-50Gy/3-4 fractions, administered once daily. FBCT and 4DCT will be acquired.

Conventional SBRTradiation

SBRT with PTV expansion. The total dose will be 45-50Gy/3-4 fractions, administered once daily. CBCT will be acquired.