HD+ I-scan Bronchoscopy Vascular Abnormalities Detection Multicenter Study (i-scan)

Radboud University Medical Center

Status: Completed

Conditions: Lungcancer

Treatments: Device: Pentax EB-1990i HD-bronchoscope guided biopsy

Study type: Observational

Funder types: Other

Identifiers

NCT02285426

NL5012109114

Details and patient eligibility

About

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.

Full 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.

Enrollment: 134 patients

Sex: All

Ages: 18 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with indication for diagnostic bronchoscopy for suspected or proven lung cancer.
• ASA physical status 1-3.
• Age 18 years or older.
• Signed and dated patient informed consent.

Exclusion criteria

• Bleeding disorders.
• Indication for use of anticoagulant therapy (acenocoumarol, warfarin, therapeutic dose of low molecular weight heparines or clopidrogel).
• Known allergy for lidocaine.
• Known pulmonary hypertension.
• Recent and/or uncontrolled cardiac disease.
• Compromised upper airway (eg concomitant head and neck cancer or central airway stenosis for any reason).
• ASA classification greater than or equal to 4.
• Pregnancy.
• Inability to consent.

Trial design

134 participants in 1 patient group

suspected lungcancer

Description:

Patients will undergo a bronchoscopy with the Pentax EB1990i HD-bronchoscope investigating the entire bronchial tree. The HD+ bronchoscopy needs to be performed in a standardized way using 3 different imaging modes: 1. HD+bronchoscopy 2. HD+bronchoscopy + i-Scan 1 3. HD+bronchoscopy + i-Scan 2

Treatment:

Device: Pentax EB-1990i HD-bronchoscope guided biopsy