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NCT04883697 Clinical Trial

Retrospective Evaluation of Risk Factors for Lower Outcomes After Vitrectomy With ILM Flap Technique

Macular Holes Clinical Trial

Official title:
Retrospective Evaluation of Risk Factors for Lower Outcomes After Vitrectomy With ILM Flap

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04883697
Other study ID # RAI
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date May 1, 2021

Study information
Verified date May 2021
Source Vienna Institute for Research in Ocular Surgery
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A retrospective review of medical charts of patients having undergone vitrectomy with ILM Peeling and ILM flap technique for macular hole repair.

Description:

A retrospective review of medical charts of patients having undergone vitrectomy with ILM Peeling and ILM flap technique for macular hole repair. Pre- and postoperative OCT and visual acuity in the time period up to 6 months after surgery are reviewed and possible risk factors for failed macular hole closure or lower visual acuity outcome after surgery are assessed.

Recruitment information / eligibility
Status Completed
Enrollment 71
Est. completion date May 1, 2021
Est. primary completion date May 1, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years to 105 Years
Eligibility Inclusion Criteria: - Vitrectomy with ILM peeling and ILM flap technique in the time period form 1.1.2015 to 31.4.2020 - Age 18 or older Exclusion Criteria: - Age <18

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• vitrectomy with ILM peeling and ILM flap technique
outcomes after vitrectomy with ILM peeling and ILM flap technique for macukar hole repair are assessed

Locations
Country Name City State
Austria Vienna Institute for Research in Ocular Surgery Vienna

Sponsors (1)
Lead Sponsor Collaborator
Vienna Institute for Research in Ocular Surgery

Country where clinical trial is conducted

Austria, 

Outcome
Type Measure Description Time frame Safety issue
Primary visual acuity best corrected distance visual acuity change between visual acuity 2-6 months postoperative to baseline
Primary macular hole closure closure of the macular hole assesed with OCT 2-6 months postoperative
See also
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