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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03809585
Other study ID # 6612-IRIS
Secondary ID R01EY028755
Status Recruiting
Phase
First received
Last updated
Start date June 20, 2018
Est. completion date December 2025

Study information

Verified date February 2024
Source Oregon Health and Science University
Contact Denzil Romfh, OD
Phone 503-494-4351
Email romfhd@ohsu.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is an observational study using OCT angiography to assist with tumor characterization in melanotic and amelanotic iris lesions. OCT angiography data from healthy eyes will be compared to eyes with various types of iris tumors.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2025
Est. primary completion date December 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria for tumor group: - Eyes with diagnosis of melanotic or amelanotic iris tumors Inclusion Criteria for healthy control group: - Eyes without iris defects or lesions Exclusion Criteria (both groups): - Inability to give informed consent - Inability to maintain stable fixation for OCT imaging - Inability to commit to required study visits - Eyes with concurrent retinal diseases, glaucoma, or conditions that in the opinion of the investigators might affect iris circulation - Mature cataracts if found to limit visual potential to worse than 20/40

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Oregon Health & Science University Portland Oregon

Sponsors (2)

Lead Sponsor Collaborator
Oregon Health and Science University National Eye Institute (NEI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tumor Thickness in Benign vs Malignant Iris Lesions OCT/OCTA will be used to compare tumor thickness measurements against the conventional Ultrasonic Biomicroscopy (UBM) device. Tumor thickness will be measured in millimeters, and growth of 0.5 mm or greater will be used to differentiate malignant from benign lesions. 6 months
Secondary Tumor Area in Benign vs Malignant Iris Lesions Tumor area will be measured by OCT/OCTA in mm2 and compared against conventional UBM measurements. 6 months
Secondary Tumor Volume in Benign vs Malignant Iris Lesions Tumor volume will be measured by OCT/OCTA in mm3 and compared against conventional UBM measurements. 6 months
Secondary Effect of Radiation Treatment on Tumor and Surrounding Ocular Structures Vessel density and tortuosity will both be measured in % occupied by flow pixels on OCT/OCTA. 6 months after treatment