WithdrawnPhase 1NCT02653612

Intraoperative Imaging of Pulmonary Adenocarcinoma

The goal is to improve surgery by preventing tumor cells from being left behind at the time of surgery. This includes finding residual tumor cells in the wound after surgery.

Checked against the public recordLast updated Mar 2, 2018 · Source: ClinicalTrials.gov

StatusWithdrawn
PhasePhase 1
U.S. locations1
SponsorVA Office of Research and Development
01
Study overview

What this study is about

Purpose
Diagnostic
Study type
Interventional
Phase
Phase 1
Sponsor
VA Office of Research and Development
Interventions being studied
Drug: EC17 imaging contrast agent
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

Inclusion Criteria: * lung cancer * surgical candidate * operable * resectable Exclusion Criteria: \- no allergies to contrast dyes

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

  • Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PAPhiladelphia, Pennsylvania

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Mar 2, 2018. Always confirm current availability with the study team.

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