New imaging technique could let doctors see lung Cancer's inner workings in real time
NCT ID NCT02676050
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early-phase study tested whether two optical imaging agents could be used during a bronchoscopy to visualize activated neutrophils and a cancer-related protein called c-MET in lung tumors. Five participants with lung cancer received the agents through a special catheter while doctors used a miniaturized imaging fiber to detect signals. The goal was to explore whether this technique could provide real-time molecular insights into lung cancer, but the study was terminated early and was not designed to treat the disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Optical imaging agents (EMI-137 and NAP)
- What this could lead to
- If successful, this approach could help doctors see specific cancer-related molecules in real time during a lung exam, potentially improving diagnosis or treatment guidance.
- What could go wrong
- This was a very small, early exploratory study that was terminated early. It was designed only to test imaging feasibility, not to treat or cure lung cancer.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
-
5 people
The number who actually took part.
- Started
-
Oct 2019
- Finished
-
Mar 2022
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
16 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
INCLUSION CRITERIA FOR COHORT 1 • Patients undergoing cardiothoracic surgery for resection of lung cancer INCLUSION CRITERIA FOR COHORT 2 • Patients with inoperable stage 3 or 4 lung cancer INCLUSION CRITERIA FOR BOTH COHORTS * ≥ 16 years * Provision of informed consent from the patient prior to any study related procedures. * Normal electrocardiogram (ECG) * Forced Expiratory Volume (FEV1) \>1L * Thoracic CT scan taken in the last 20 weeks * Attending consultant permission for bronchoscopy * Readily accessible target areas with bronchoscopy and FE EXCLUSION CRITERIA * Refusal for participation by attending consultant * Unsuitable for bronchoscopy * Any history of anaphylaxis * Significant coagulopathy, which causes bronchoscopy to be unsuitable, as determined by clinical co-investigator or the participant's attending consultant, using information which is routinely available * Myocardial infarction in the preceding four weeks * Women who are pregnant or are breastfeeding * Receiving drugs that cause increased autofluorescence in the lung, specifically amiodorane and methotrexate * Oxygen saturation \<92% breathing room air * Platelet count \< 50 x 109/L * Bleeding diathesis
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Royal Infirmary of Edinburgh
Edinburgh, EH16 4TJ, United Kingdom
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