Phase
Condition
N/ATreatment
Postoperative intraocular tamponade
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Primary MH ≤250 μm
MH duration ≤12 months
No previous vitreoretinal surgery in study eye
Ability to sign informed consent
Signed informed consent
Age ˃18 years
Exclusion
Exclusion Criteria:
Previous vitreoretinal surgery in study eye
Secondary MH caused by other conditions than vitreomacular traction
Myopic MH, i.e., excessive myopia (more than -6 dioptres)
Traumatic MH
MH secondary to retinal detachment or other retinal diseases
Previously participation in this study
Study Design
Connect with a study center
Department of Ophthalmology, University of Thessaly
Thessaly, 38221
GreeceSite Not Available
Stavanger University Hospital
Stavanger, Rogaland 4026
NorwayActive - Recruiting
University Hospital of Northern Norway
Tromsø, Troms 9019
NorwayActive - Recruiting
St. Olavs University Hospital
Trondheim, Tronderlag 7030
NorwayActive - Recruiting
Haukeland University Hospital
Bergen, Vestland 5021
NorwayActive - Recruiting
Oslo University Hospital
Oslo, 0424
NorwayActive - Recruiting
Clinical Universitary Hospital of Santiago
Santiago De Compostela, La Coruna 15706
SpainActive - Recruiting
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