Evaluation of innovative OCT techniques in comparison to conventional OCT

Not Applicable

• Conditions: H35.3; Degeneration of macula and posterior pole

• Registration Number: DRKS00013755
• Lead Sponsor: Medizinisches Laserzentrum Lübeck

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-03-14
• Study Completion: 2020-03-12
• Results First Posted: 2020-12-21
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 97

Inclusion Criteria

Persons during ophthalmologic examination requiring myriatic eye drop installation and OCT examination

Exclusion Criteria

Inability to give informed consent, mental disability, under 18 years of age, pregnancy/breast-feeding

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rate of successful self-measurement after prior instruction from the physician

Secondary Outcome Measures

Name	Time	Method
Grading of OCT images of both devices. The images will be presented in a randomized order without patient identification. <br>- Grading of image quality<br>- Sensitivity and specificity in the detection of retinal pathologies, above all intraretinal fluid (IRF), subretinal fluid (SRF), pigment epithelium detachments (PED)