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Spots Global Cancer Trial Database for HD+ I-scan Bronchoscopy Vascular Abnormalities Detection Multicenter Study

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Trial Identification

Brief Title: HD+ I-scan Bronchoscopy Vascular Abnormalities Detection Multicenter Study

Official Title: A Multicenter Study Evaluating the Diagnostic Value for Vascular Abnormalities of High Definition Bronchoscopy When Combined With I-scan Imaging Technology Compared to High Defintion Bronchoscopy Alone

Study ID: NCT02285426

Conditions

Lungcancer

Study Description

Brief Summary: Videobronchoscopy is an essential diagnostic procedure for evaluation of the central airways and pivotal for the diagnosis and staging of lung cancer. Further technological improvements have resulted in high definition (HD+) images and advanced image enhancement technique (i-scan). An earlier study (NCT01676012) has indicated that HD+ bronchoscopy in combination with i-scan technology is superior to HD+WL (white light) for detecting endobronchial vascular changes. In this study we aim to correlate these vascular changes to histology and hypothesize that these vascular changes are related to (pre-) malignant changes and that the addition of i-scan is superior to HD+ WL.

Detailed Description: Patients will undergo a bronchoscopy with Pentax EB1990i HD-bronchoscope in combination with Pentax EPKi series videoprocessor investigating the entire bronchial tree. Bronchoscopy will be performed by an experienced chest physician under local anaesthesia use and type of sedation following local protocol. Bronchoscopy will be performed in a standardized order using three different imaging modes. The order of the different modes will be randomized to avoid induced scope and / or cough lesion bias. High definition digital videos will be made from all procedures without in screen patient identification, but using a study code. The three imaging modes used in this study are: HD+, HD+ surface enhancement (SE, i-scan1) and HD+ surface enhancement and tone enhancement (TE-c, i-scan2). When sites with abnormal or suspicious vascular patterns are detected the investigator grade these findings using a visual classification scale \[adapted from Herth JTO 2009 \& Zaric Med Oncol 2013\] and change to a regular bronchoscope and take biopsies from each site and a biopsy from a normal secondary carina on the contralateral site as control. Finally any other indicated procedures will be performed at the discretion of the local investigator.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Ospedale Umberto I, Via Dante Alighieri n.1, Ravenna, RA, Italy

RadboudUMC, Nijmegen, Gelderland, Netherlands

St-Petersburg Research Institute of TB and Thoracic Surgery, Saint-Petersburg, , Russian Federation

Hospital Universitario Santa Lucia, Murcia, , Spain

Contact Details

Name: Erik HF van der Heijden, MD, PhD

Affiliation: Principal Investigator

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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