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Thin-EBUS in Ex-vivo Human Lungs

University Health Network, Toronto logo

University Health Network, Toronto

Status

Completed

Conditions

Lung Cancer

Treatments

Device: Thin Convex Probe Endobronchial Ultrasound (TCP-EBUS)

Study type

Interventional

Funder types

Other

Identifiers

NCT03349307
16-6083

Details and patient eligibility

About

This study will determine the feasibility of the novel thin convex probe endobronchial ultrasound (TCP-EBUS) in human resected lobes. The primary end point is to clarify the feasibility of using the thin convex probe EBUS scope to visualize lung tumors from an intra-bronchial view. The secondary objective is to evaluate the insertion ability, operability, endoscopic image and ultrasound image compared to that of the convex probe EBUS.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any patients scheduled for lobectomy or anatomical segmental resection for malignant lung tumors.
  • 18 years of age or older

Exclusion criteria

  • Any patients with inability to give informed consent.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

No Intervention
Experimental group
Treatment:
Device: Thin Convex Probe Endobronchial Ultrasound (TCP-EBUS)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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