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Hyperspectral Endoscopy Imaging for the Early Detection of Precancerous Lesions in Average Risk Patients

OHSU Knight Cancer Institute logo

OHSU Knight Cancer Institute

Status

Completed

Conditions

Patient

Treatments

Procedure: Hyperspectral Endoscopy (HySE)
Device: White Light Endoscopy (WLE)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04172493
NCI-2019-06087 (Registry Identifier)
ONC-19132-L
P30CA069533 (U.S. NIH Grant/Contract)
STUDY00018947 (Other Identifier)

Details and patient eligibility

About

This trial studies whether hyperspectral endoscopy improves visualization of abnormal tissue in average risk patients during standard-of-care colonoscopies. Hyperspectral endoscopy is an emerging technique that has the potential to enable the signals from blood to be resolved from tissue-specific signals. Image-enhanced endoscopy may improve visualization of abnormal colonic tissue when compared to the standard-of-care high-definition white light endoscopy.

Full description

PRIMARY OBJECTIVE:

I. To assess whether use of hyperspectral endoscopy (HySE) can improve visualization of abnormal colonic tissue.

SECONDARY OBJECTIVES:

I. To assess whether use of HySE could reduce the rate of missed flat polyps.

II. To assess whether use of HySE might in the future reduce the incomplete resection rate (IRR).

III. To examine accuracy of practitioners in predicting polyp histology.

OUTLINE:

Patients undergo standard of care white light endoscopy and hyperspectral endoscopy during routine colonoscopy procedure.

After completion of study, patients who experience a colonoscopy-related severe adverse event are followed up until resolution or stabilization of the event.

Enrollment

13 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Ability to understand and the willingness to sign a written informed consent document
  • Patients scheduled for a standard of care screening or surveillance colonoscopy

Exclusion criteria

  • Any condition that, in the opinion of the investigator, precludes the patient from completion of the study procedure

Trial design

Primary purpose

Device Feasibility

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

13 participants in 1 patient group

Diagnostic
Experimental group
Description:
Patients undergo standard of care white light endoscopy (WLE) and hyperspectral endoscopy (HySE) during routine colonoscopy procedure.
Treatment:
Device: White Light Endoscopy (WLE)
Procedure: Hyperspectral Endoscopy (HySE)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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