nCLE-guided bronchoscopy for peripheral lung cancer diagnosis; a Randomized Controlled Trial
Descrizione riassuntiva dello studio
Tumors in the lung can have various causes and can be either benign or malignant. X-rays or CT scans often cannot definitively determine what type of lung tumor it is. Therefore, in most cases, a bronchoscopy is necessary, where tissue is obtained from the tumor using needles, forceps, or cryoprobes, allowing for identification of the tumor type. However, the difficulty with this examination can sometimes be that the tumor cannot be accurately located, and the tissue samples are therefore not taken from the correct, optimal site. New techniques are continuously being introduced to help the physician find the optimal position for tissue sampling. One such technique is confocal laser endomicroscopy (CE-certified), which allows for direct visualization of tumor cells. This can give the physician more confidence that they have found the optimal position for tissue sampling. The physician inserts a needle into the tumor, which contains a CLE probe. After visualizing the tumor cells, the CLE probe is removed from the needle, and the physician can then directly obtain the tumor cells with the needle. Additionally, tissue samples are also taken using forceps or the cryoprobe at the examiner's discretion. This is not study-related but clinically necessary, as the goal is to obtain as much tissue as possible for diagnosis. Currently, it is not known whether the use of such a CLE probe truly increases diagnostic accuracy. This question will be addressed in this study.
(BASEC)
Intervento studiato
As part of standard care, a bronchoscopy will be performed through the trachea. A sedative will be administered via an infusion in the arm so that patients do not notice anything during the examination.
For the study, we will apply the CLE technique as an adjunct to bronchoscopy in 50% of the participants.
We will form two groups for this study:
• Group 1: Participants in this group will undergo regular bronchoscopy without additional CLE technique.
• Group 2: Participants in this group will undergo the CLE technique in addition to regular bronchoscopy.
The two examination groups will be selected randomly. Before the bronchoscopy begins, they will not know which group they have been assigned to.
The bronchoscopy is performed for medical reasons, not study-related. Patients will be informed separately about the bronchoscopy and its risks. The bronchoscopy will proceed as follows: While they are asleep, the physician will locate the lung tumor as usual and insert a needle into it for a tissue sample.
The only difference from the "standard treatment" is that during the bronchoscopy, a CLE probe will be temporarily inserted into the tumor to visualize the tumor cells. Fluorescein will be injected into the vein so that the tumor cells can be seen using the CLE probe. This will extend the bronchoscopy by about 10 minutes. Otherwise, the bronchoscopy and the entire treatment do not differ from the clinical standard.
After the bronchoscopy, patients will remain in the recovery room for about 1.5 hours, which corresponds to the standard protocol after a normal bronchoscopy. Patients do not need to come for an additional hospital visit.
(BASEC)
Malattie studiate
Peripheral lung cancer
(BASEC)
• Over 18 years old • Suspicion of malignant peripheral lung lesion with indication for bronchoscopy • Solid part of the lesion must be >10 mm in size • Largest extent of the lesion in CT ≤30 mm • Bronchial signs in CT before the procedure or estimated probability of successful navigation to the node leading to an r-EBUS signal • Ability to understand and willingness to sign a written informed consent (BASEC)
Criteri di esclusione
• Inability or unwillingness to provide informed consent • Patients with an endobronchial, visible lung tumor during bronchoscopy • Patients for whom the target lesion is within reach of the linear EBUS endoscope • Non-compliance with the study protocol • Patients with known allergy to fluorescein or risk factors for an allergic reaction • Pregnant or breastfeeding women • Patients with hemodynamic instability • Patients with refractory hypoxemia • Patients on a therapeutic anticoagulant that cannot be held for an appropriate period before the procedure • Patients undergoing chemotherapy, as multiple chemotherapies at the same wavelength have fluorescent properties • Inability to follow up (BASEC)
Luogo dello studio
Basilea
(BASEC)
Sponsor
University Hospital Basel
(BASEC)
Contatto per ulteriori informazioni sullo studio
Persona di contatto in Svizzera
Dr. Jürgen Hetzel
+41613286195
juergen.hetzel@clutterusb.chUniversity Hospital Basel, pneumology,
(BASEC)
Informazioni scientifiche
non disponibile
Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)
Commissione d'etica svizzera nord-ovest/centrale EKNZ
(BASEC)
Data di approvazione del comitato etico
24.06.2025
(BASEC)
ID di studio ICTRP
non disponibile
Titolo ufficiale (approvato dal comitato etico)
nCLE-guided bronchoscopy for peripheral lung cancer diagnosis; a Randomized Controlled Trial (BASEC)
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