NCT00564291

Brief Summary

Comparison of different OCT instruments to assess retinal thickness, correlation to fluorescein angiography, and visual outcome after therapy with anti-VEGF therapy

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
700

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2007

Longer than P75 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2007

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

November 26, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 27, 2007

Completed
16 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 27, 2023

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 28, 2023

Completed
Last Updated

November 29, 2023

Status Verified

November 1, 2023

Enrollment Period

16.9 years

First QC Date

November 26, 2007

Last Update Submit

November 28, 2023

Conditions

Keywords

OCT

Outcome Measures

Primary Outcomes (1)

  • Integrity of retinal layers

    End of study

Study Arms (7)

1

Healthy volunteers

Other: Examination with an OCT device

2

CSME secondary to diabetic retinopathy

3

ARMD with CNV before and after therapy

Other: Examination with an OCT device

4

ARMD atrophic

Other: Examination with an OCT device

5

Retinal vein occlusion

Other: Examination with an OCT device

6

retinitis pigmentosa

Other: Examination with an OCT device

7

vitreoretinal proliferation

Other: Examination with an OCT device

Interventions

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

healthy subjects and patients with macular diseases

You may qualify if:

  • Macular disease
  • Healthy subjects

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Dep. Ophthalmology, University Hospital Bern

Bern, 3010, Switzerland

Location

Klinik und Poliklinik für Augenheilkunde, University Bern

Bern, Switzerland

Location

Related Publications (3)

  • Lincke JB, Keller S, Amaral J, Zinkernagel MS, Schuerch K. Ciliary body length revisited by anterior segment optical coherence tomography: implications for safe access to the pars plana for intravitreal injections. Graefes Arch Clin Exp Ophthalmol. 2021 Jun;259(6):1435-1441. doi: 10.1007/s00417-020-04967-3. Epub 2020 Oct 19.

  • Wolf-Schnurrbusch UE, Ghanem R, Rothenbuehler SP, Enzmann V, Framme C, Wolf S. Predictors of short-term visual outcome after anti-VEGF therapy of macular edema due to central retinal vein occlusion. Invest Ophthalmol Vis Sci. 2011 May 18;52(6):3334-7. doi: 10.1167/iovs.10-6097.

  • Rothenbuehler SP, Waeber D, Brinkmann CK, Wolf S, Wolf-Schnurrbusch UE. Effects of ranibizumab in patients with subfoveal choroidal neovascularization attributable to age-related macular degeneration. Am J Ophthalmol. 2009 May;147(5):831-7. doi: 10.1016/j.ajo.2008.12.005. Epub 2009 Feb 13.

MeSH Terms

Conditions

Macular Edema

Interventions

Restraint, Physical

Condition Hierarchy (Ancestors)

Macular DegenerationRetinal DegenerationRetinal DiseasesEye Diseases

Intervention Hierarchy (Ancestors)

Behavior ControlTherapeuticsImmobilizationInvestigative Techniques

Study Officials

  • Sebastian Wolf, MD, PhD

    University of Bern

    PRINCIPAL INVESTIGATOR
  • Sebastian Wolf, MD PhD

    University of Bern

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Director

Study Record Dates

First Submitted

November 26, 2007

First Posted

November 27, 2007

Study Start

January 1, 2007

Primary Completion

November 27, 2023

Study Completion

November 28, 2023

Last Updated

November 29, 2023

Record last verified: 2023-11

Locations