TerminatedNot applicableNCT02745548
Official study title

Bronchial Mapping (GCC 1635)

Study summary

In order to better understand radiation-induced lung toxicity, the investigator proposes a novel functional avoidance approach that incorporates central as well as peripheral BSS segments in the treatment planning process in order to quantify and account for their respective radiosensitivities. Specifically, the investigator proposes a systematic study that involves acquiring pre- and post-SAbR high-resolution CT and SPECT V/Q scans from lung cancer patients who receive radiotherapy, followed by auto-segmentation of the BSS elements using virtual bronchoscopy.

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Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studiedNot specified

The study team can explain what participation involves.

Who it may be forThoracic Cancer

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated May 15, 2025 · Source: ClinicalTrials.gov

Is enrollment open?Terminated

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?University of Maryland, Baltimore

Study sponsor

01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
University of Maryland, Baltimore
Interventions being studied
Not specified
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Treatment approach
03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Patients with primary or metastatic lung lesions to be treated using stereotactic ablative radiotherapy (There is no limitation on the location or number of lesions for this study) OR Conventionally fractionated RT patients with primary or metastatic lung lesions
  • Age ≥ 18 years. No gender or ethnic restrictions.
  • Performance status ECOG ≥ 3
  • Ability to hold breath for \~20 seconds
  • Ability to understand and the willingness to sign a written informed consent.
  • Any types and amounts of prior therapy will be allowed for this study.
  • Maximum PTV dimension ≤ 70 mm
Reasons someone may not be able to joinExclusion criteria
  • Children (age \<18 years).
  • Women who are pregnant, nursing, or trying to get pregnant.
  • ECOG performance status \< 3

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Ummc MsgccBaltimore, Maryland

Source and freshness
Processed from ClinicalTrials.gov. Last public update: May 15, 2025. Always confirm current availability with the study team.

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