Evidence map›Paper›PMID 42045970›Full record

ArticleTrials2026

Labelling of subpleural pulmonary nodules with blue dye and contrast agents under CT-guided control and subsequent video-assisted thoracoscopic resection: the BLUEPAT prospective randomised study.

Zdeněk Chovanec, Vladimír Červeňák, Ivan Čundrle, Michal Šitina, Jiří Vaníček, Alena Berková, Tomáš Hanslík, Igor Penka, Lenka Součková

Abstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Zdeněk Chovanec1 st Department of Surgery, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
Vladimír Červeňák1 st Department of Surgery, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
Ivan ČundrleDepartment of Anaesthesiology and Resuscitation, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
Michal ŠitinaDepartment of Anaesthesiology and Resuscitation, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
Jiří Vaníček1 st Department of Surgery, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
Alena Berková1 st Department of Surgery, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
Tomáš Hanslík1 st Department of Surgery, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
Igor Penka1 st Department of Surgery, Faculty of Medicine, Masaryk University and St. Anne's University Hospital, Brno, Czech Republic.
Lenka SoučkováInternational Clinical Research Center, St. Anne's University Hospital, Brno, Czech Republic. lsouckova@med.muni.cz.ORCID http://orcid.org/0000-0003-0028-4464

Funding

CZECRIN LM2023049
6 · The paper itself

Abstract

backgroundColour marking of indicated nodules is an innovative, accurate, and gentle method that allows subsequent wedge resection of the marked tissue using a mini-invasive, video-assisted thoracoscopic (VATS) method with all its benefits. One of the expected benefits of this clinical trial is introducing and optimising the evaluated way into routine management in diagnosing and treating focal lung diseases. The BLUEPAT clinical trial aims to assess the technique of colour marking of subpleural deposited small lung nodules with the subsequent performance of VATS wedge resection in surgical practice.

methodsThe BLUEPAT clinical trial is a prospective, monocentric, open-label, randomised study that will include 72 participants with subpleural deposited nodules with the need for additional histological diagnostics to optimise subsequent treatment. These patients will be randomised into two arms in a 1:1 ratio. The interventional arm will undergo VATS wedge resection of lung nodules marked with Patent Blue V and contrast agent iohexol under CT-guided control. The control arm will undergo VATS resection without prior colour coding of the lung nodules. The feasibility and safety of both methods will be assessed based on the evaluation of the parameters of the primary and secondary objectives of the study. The safety of the methods will be monitored by recording all related adverse events. All enrolled patients will undergo a 30-day follow-up period within the framework of clinical trial.

resultsThis article reports the clinical trial protocol; outcome data will be published upon study completion. DISCUSSION: The BLUEPAT clinical trial offers a novel assessment of this innovative approach for the diagnosis and treatment of focal lung diseases. The use of patent blue dye has been well established in diagnostic procedures for breast cancer and this study extends its potential application to pulmonary indications.

trial registrationEudraCT Number 2021-001122-22. Registered on March 18, 2021.

Indexed as

Coloring AgentsContrast MediaPneumonectomyRadiography, InterventionalSolitary Pulmonary NoduleThoracic Surgery, Video-AssistedTomography, X-Ray ComputedFemaleHumansIohexolMultiple Pulmonary NodulesProspective StudiesRandomized Controlled Trials as TopicRosaniline DyesTreatment OutcomeColoring AgentsContrast MediaIohexolRosaniline DyesContrast agent iohexolCT-guidedDiagnosis and treatment of focal lung diseasesPatent blueVideo-thoracoscopic resection

Identifiers

PMID42045970
PMCPMC13255219

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.