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NCT03922932 · ClinicalTrials.gov registry record

WF and PR OCTA in Diabetic Retinopathy

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

Active
Registry status
290
Enrollment target
1
Study location

NCT03922932 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 290 participants, below the 1,671-participant average among 57 other Diabetic Retinopathy trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03922932, a study of Diabetic Retinopathy, is active but no longer recruiting, sponsored by Oregon Health and Science University.

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

Study Summary

Diabetic retinopathy (DR) is a leading cause of vision loss in working-age Americans. Capillary damage from hyperglycemia causes vision loss through downstream effects, such as retinal ischemia, edema, and neovascularization (NV). Proper screening and timely treatment with laser photocoagulation and anti-vascular endothelial growth factor (VEGF) injections can minimize morbidity. In the last decade, clinicians have been able to use objective structural data from optical coherence tomography (OCT) to guide the treatment of diabetic macular edema. Other aspects of care, however, still largely depend on subjective interpretation of clinical features and fluorescein angiography (FA) to determine the disease severity and treatment threshold. The recently developed OCT angiography (OCTA) provides dye-less, injection-free, three-dimensional images of the retinal and choroidal circulation with high capillary contrast. Not only is it safer, faster, and less expensive than conventional dye-based angiography, OCTA provides the potential of giving clinicians objective tools for determining severity of disease by detecting and quantifying NV and non-perfusion.

Conditions Studied

Study Locations (1)

Oregon

  • Oregon Health & Science University - Portland

Trial Details

FieldValue
Enrollment Target 290 participants
Start Date 2017-08-30
Est. Completion 2027-12

What the Registry Record Tells You About NCT03922932

The ClinicalTrials.gov registry entry for NCT03922932 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 290 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,671-participant average among 57 other Diabetic Retinopathy trials with a reported enrollment target (83% 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.

NCT03922932 reports 1 study location spanning 1 distinct geographic area - top geographies include Oregon.

Frequently Asked Questions

What is clinical trial NCT03922932 about?

NCT03922932 is a clinical study titled "WF and PR OCTA in Diabetic Retinopathy". Diabetic retinopathy (DR) is a leading cause of vision loss in working-age Americans. Capillary damage from hyperglycemia causes vision loss through downstream effects, such as retinal ischemia, edema, and neovascularization (NV). Proper screening and timely treatment with laser photocoagulation and...

What is the current status of trial NCT03922932?

This trial is currently active not recruiting. The enrollment target is 290 participants. The study started on 2017-08-30. Estimated completion is 2027-12.

What conditions does trial NCT03922932 study?

This clinical trial studies the following conditions: Diabetic Retinopathy.

Who is sponsoring clinical trial NCT03922932?

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

Where is trial NCT03922932 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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