Evaluation of innovative OCT techniques in comparison to conventional OCT

Evaluation of innovative OCT techniques in comparison to conventional OCT - Evokon

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00013755

Enrollment

102

Registered

2018-03-14

Start date

2018-03-19

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

H35.3

Interventions

Group 1: Examination of the retina of patients with (suspected) retinal disease with standard OCT and new Full-Field-OCT

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Persons during ophthalmologic examination requiring myriatic eye drop installation and OCT examination

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Rate of successful self-measurement after prior instruction from the physician	—

Secondary

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

Countries

Germany

Contacts

Public ContactClaus von der Burchard

Universitätsaugenklinik Kiel

claus.vonderburchard@uksh.de+49 431 500 24201

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 24, 2026