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Optical Coherence Tomography in Staging Patients With Upper Tract Urothelial Cancer

Case Comprehensive Cancer Center (Case CCC) logo

Case Comprehensive Cancer Center (Case CCC)

Status

Withdrawn

Conditions

Kidney/Urinary Cancer

Treatments

Device: optical coherence tomography

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02108587
CASE11811
P30CA043703 (U.S. NIH Grant/Contract)
NCI-2014-00347 (Registry Identifier)
CASE 11811 (Other Identifier)

Details and patient eligibility

About

This clinical trial studies how well optical coherence tomography works in staging patients with upper-tract urothelial carcinomas. Staging describes the severity of a person's cancer based on the size and/or extent (reach) of the original (primary) tumor and whether or not cancer has spread in the body. It also helps the doctor plan the appropriate treatment. Optical coherence tomography is a procedure that uses infrared light waves to give three-dimensional pictures of structures inside tissues and organs. The pictures are made by a computer linked to the light source. Optical coherence tomography may be effective in staging patients with upper-tract urothelial carcinomas.

Full description

PRIMARY OBJECTIVES:

I. To test the feasibility and imaging ability of optical coherence tomography (OCT) to stage upper-tract urothelial carcinomas (UTUC).

OUTLINE:

Patients undergo optical coherence tomography over 10-15 minutes.

After completion of study, patients are followed up at 3 months.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients must have radiographic evidence of upper tract urothelial cancer by computed tomography (CT), magnetic resonance imaging (MRI) or intravenous pyelogram (IVP) in order to undergo this procedure
  • Patient who will undergo standard of care clinical staging for UTUC
  • Patient ability to read and comprehend the informed consent document

Exclusion criteria

  • Patient who has a contraindication to endoscopy
  • Patient who is pregnant

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

optical coherence tomography for diagnosis
Experimental group
Description:
Patients undergo optical coherence tomography over 10-15 minutes.
Treatment:
Device: optical coherence tomography

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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