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Structural Imaging Assisted Retinal Fluorescence Lifetime Imager (STARFLI)

I

Insel Gruppe AG, University Hospital Bern

Status

Not yet enrolling

Conditions

Retinal Disease

Treatments

Device: OCT/FLIM

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT05819307
STARFLI

Details and patient eligibility

About

To investigate the feasibility of a combined OCT/FLIM device

Full description

To investigate the feasibility of a combined Optical coherence tomography/ Fluorescence Lifetime Measurement (OCT/FLIM) device.

Enrollment

70 estimated patients

Sex

All

Ages

18 to 120 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subject must be willing to give written informed consent
  • Age: Patients and Probands 18 years or greater
  • Both eyes will be assessed in the study

Exclusion criteria

  • Patients not willing or able to sign informed consent
  • Patients younger than 18 years
  • Patients with epilepsy

Trial contacts and locations

1

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Central trial contact

Pia Steinger

Data sourced from clinicaltrials.gov

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