Macular Holes Clinical Trial
Official title:
Randomized Clinical Trials to Compare the Healing Process of Idiopathic Macular Hole With Different Surgical Techniques
To compare anatomic and functional results, and to evaluate postoperatively the healing process in 2 different techniques for the closure of the macular holes (MH)
Patients with macular holes classified in stages 3 and 4 will be randomized into 2 groups. .
In Group A, patients will undergo peeling with complete removal of the internal limiting
membrane (ILM) and in the group B, the inverted ILM peeling technique will be performed. The
20% sulfur hexafluoride (SF6) gas will be used as a tamponade agent in all surgeries, and
patients will be instructed to avoid the prone position for 5 days.
OCT images will be performed in the first 5 postoperative days and months 1, 3 and 6.
The primary outcome is anatomic closure of the MH closure in the month 6. The second outcomes
are: mean best corrected visual acuity (BCVA) at month 6, mean change in the BCVA at month 6;
integrity of the perifoveal external limiting membrane and ellipsoid zone on Optical
Coherence Tomography (OCT); MH closure rate over time in days; functional improvement of
microperimetry Statistical analysis will be performed with Student t-test and the p-value of
≤ 0.05 is considered significant.
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