Trials / Completed
CompletedNCT03912584
Study Comparing the P200TE and the P200TxE in Glaucoma Patients
Qualitative OCT Image Grading Study Comparing the P200TE and the P200TxE in Glaucoma Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Optos, PLC · Industry
- Sex
- All
- Age
- 22 Years
- Healthy volunteers
- Not accepted
Summary
The study evaluates the image quality between two OCT devices.
Detailed description
The objective of this study is to collect OCT scans to compare the qualitative B scan images produced by the P200TxE to the P200TE device in glaucoma subjects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | P200TE | The P200TE Ophthalmoscope provides widefield Scanning Laser Ophthalmoscope (SLO) fundus imaging and Optical Coherence Tomography (OCT) imaging in one device. |
| DEVICE | P200TxE | The P200TxE Ophthalmoscope provides widefield Scanning Laser Ophthalmoscope (SLO) fundus imaging and Optical Coherence Tomography (OCT) imaging in one device. |
Timeline
- Start date
- 2019-04-29
- Primary completion
- 2019-04-30
- Completion
- 2019-04-30
- First posted
- 2019-04-11
- Last updated
- 2022-09-23
- Results posted
- 2022-09-23
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03912584. Inclusion in this directory is not an endorsement.