Visual Acuity and Optical Coherence Tomography One Year After Peeling of Epiretinal Membranes

Sponsor
Vienna Institute for Research in Ocular Surgery (Other)
Overall Status
Recruiting
CT.gov ID
NCT03583632
Collaborator
(none)
20
1
46.9
0.4

Study Details

Study Description

Brief Summary

Improvement in visual acuity and retinal anatomy one year after surgery is assessed and compared to data preoperative and 3 months after surgery

Condition or Disease Intervention/Treatment Phase
  • Other: visual acuity testing
  • Device: optical coherence tomography

Detailed Description

Improvement in visual acuity and retinal anatomy (documented by optical coherence tomography) one year after surgery is assessed and compared to data preoperative and 3 months after surgery. Aim of the study is to examine possible improvements of surgical outcomes in the period up to the one year follow-up.

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Case-Control
Time Perspective:
Other
Official Title:
Visual Acuity and Optical Coherence Tomography One Year After Peeling of Epiretinal Membranes
Actual Study Start Date :
Feb 1, 2018
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Dec 31, 2021

Outcome Measures

Primary Outcome Measures

  1. visual acuity [3 minutes]

    visual acuity testing with EDTRS charts

Secondary Outcome Measures

  1. optical coherence tomography [3 minutes]

    optical coherence tomography generates slides of the retinal anatomy with light

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • vitrectomy with Membrane Peeling due to an epiretinal membrane
Exclusion Criteria:
  • none

Contacts and Locations

Locations

Site City State Country Postal Code
1 Vienna Institute for Research in Ocular Surgery (VIROS), Hanusch Hospital Vienna Vienna Austria 1140

Sponsors and Collaborators

  • Vienna Institute for Research in Ocular Surgery

Investigators

  • Principal Investigator: Oliver Findl, MD, Prof, VIROS at Hanuschkrankenhaus Vienna

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Prim. Prof. Dr. Oliver Findl, MBA, Head of the Department of Ophthalmology, Professor, Principal Investigator, Vienna Institute for Research in Ocular Surgery
ClinicalTrials.gov Identifier:
NCT03583632
Other Study ID Numbers:
  • ERM 1year follow-up
First Posted:
Jul 11, 2018
Last Update Posted:
Jan 12, 2021
Last Verified:
Jan 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 12, 2021