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NCT02330042 · ClinicalTrials.gov registry record

OCT Biomarkers for Diabetic Retinopathy

A clinical trial of Diabetic Retinopathy, sponsored by Oregon Health and Science University.

Active
Registry status
165
Enrollment target
1
Study location

NCT02330042 is a study of Diabetic Retinopathy that is active but no longer recruiting, run by Oregon Health and Science University. The registered enrollment target is 165 participants, below the 1,674-participant average among 57 other Diabetic Retinopathy trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02330042, a study of Diabetic Retinopathy, is active but no longer recruiting, sponsored by Oregon Health and Science University.

ACTIVE NOT RECRUITING
Registry status
165 participants
Enrollment target
1
Study location

Study Summary

Diabetic retinopathy (DR) is caused by changes in the blood vessels of the retina associated with long-term Type 1 or Type 2 diabetes mellitus. DR is a leading cause of blindness in the United States. Standard optical coherence tomography (OCT) cannot directly detect vascular changes, which may occur early affecting the passage of blood through the tiny capillaries (reduced capillary flow) or cause the greatest damage through formation of abnormal blood vessel growth (neovascularization). Currently, fluorescein angiography (FA) is the gold standard for detecting these changes, but FA requires an injection of a dye into the vein of the arm of the patient. This dye can cause undesirable side effects. Recently, OCT has been used to make functional measurements (such as total retinal blood flow among others) and to perform angiography. Thus, functional OCT may provide a useful, alternate way to evaluate diabetic retinopathy.

Conditions Studied

Study Locations (1)

Oregon

  • Oregon Health & Science University - Portland

Trial Details

FieldValue
Enrollment Target 165 participants
Start Date 2015-01-26
Est. Completion 2026-12

What the Registry Record Tells You About NCT02330042

The ClinicalTrials.gov registry entry for NCT02330042 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 165 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,674-participant average among 57 other Diabetic Retinopathy trials with a reported enrollment target (90% lower). The listed sponsor is Oregon Health and Science University, which has 546 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Diabetic Retinopathy appearing as the primary indexed condition, and to 0 interventions.

NCT02330042 reports 1 study location spanning 1 distinct geographic area - top geographies include Oregon.

Frequently Asked Questions

What is clinical trial NCT02330042 about?

NCT02330042 is a clinical study titled "OCT Biomarkers for Diabetic Retinopathy". Diabetic retinopathy (DR) is caused by changes in the blood vessels of the retina associated with long-term Type 1 or Type 2 diabetes mellitus. DR is a leading cause of blindness in the United States. Standard optical coherence tomography (OCT) cannot directly detect vascular changes, which may occu...

What is the current status of trial NCT02330042?

This trial is currently active not recruiting. The enrollment target is 165 participants. The study started on 2015-01-26. Estimated completion is 2026-12.

What conditions does trial NCT02330042 study?

This clinical trial studies the following conditions: Diabetic Retinopathy.

Who is sponsoring clinical trial NCT02330042?

This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02330042 being conducted?

This trial has 1 study location across Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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