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Completed

NCT Number: NCT01083056

Observational Study - ILM Peeling

This observational study investigates the effects of epimacular membrane peeling on the structure and function of the retina.

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Key information

Conditions

Epimacular Gliosis Eye Diseases Gliosis Macular Hole Pathologic Processes Pathological Conditions, Signs and Symptoms Retinal Diseases Retinal Perforations

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre for Ophthalmology, University Hospital Tuebingen

Tübingen, Baden-Wurttemberg, 72076, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of Epimacular Gliosis
  • Must be scheduled for ILM-peeling independently of study
  • Must be older then 18 years of age

Exclusion criteria

  • Visual acuity > 0,4 logMAR (< 20/50 EDTRS)
  • Other ophthalmological disorder affecting visual acuity and/or visual field and/or retinal structure

Treatment and study plan

Primary outcomes

  1. BCVA

    Time frame: 6 months after ILM peeling

Sponsors and collaborators

Lead sponsor

University Hospital Tuebingen

Other

Registry information

Official study title

Observational Study On Retinal Structure And Function Before And After Epimacular Membrane Peeling

Important dates

Study start
2010
Primary completion
2014
Study completion
2014
First posted
Mar 9, 2010
Registry last updated
Jul 31, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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