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Photometric Stereo Endoscopy (PSE) as a Tool for Imaging the Rectum and Colon

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Mass General Brigham

Status

Completed

Conditions

Colonic Polyps

Treatments

Device: PSE

Study type

Interventional

Funder types

Other

Identifiers

NCT01979458
2013P001115

Details and patient eligibility

About

The goal of this research is to assess photometric stereo endoscopy (PSE) as an endoscopic imaging technique. Specifically, topographical surface contrast reconstructed from the PSE data will be compared to conventional imaging contrast to assess if PSE provides enhanced contrast of abnormal tissue.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing a routine colonoscopy screening
  • Patients must be over the age of 18
  • Patients must be able to give informed consent

Exclusion criteria

  • Patients with bleeding/hemostasis disorders
  • Patients that are pregnant
  • Patients taking any anti-coagulants that would preclude them from undergoing a standard of care colonoscopy, such as Coumadin and Plavix, at the time of the study
  • Patients with known colitis or active bleeding will be excluded

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

PSE
Experimental group
Description:
Patients whose distal colon is imaged using the PSE device. This is a pilot trial of 30 patients.
Treatment:
Device: PSE

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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