This randomized controlled trial evaluated whether a single drop of 0.5% timolol maleate, administered before neodymium-doped yttrium aluminium garnet (Nd:YAG) laser posterior capsulotomy, reduced the rise in intraocular pressure compared with standard care alone. The study included adults aged 18-65 years who had developed posterior capsular opacification at least 3 months after cataract surgery and were scheduled to undergo Nd:YAG laser posterior capsulotomy. Participants were randomly assigned to receive either prophylactic topical timolol maleate or standard care without prophylactic timolol. Intraocular pressure was measured before the laser procedure and again 1 hour after the procedure by an ophthalmologist who was unaware of the assigned treatment. The study was based on the hypothesis that mean intraocular pressure 1 hour after posterior capsulotomy would be lower among participants who received prophylactic timolol maleate than among those who received standard care alone.
Inclusion Criteria:
Exclusion Criteria:
Participants received one drop of 0.5% timolol maleate ophthalmic solution immediately before Nd:YAG laser posterior capsulotomy. Intraocular pressure was measured before the procedure and 1 hour after capsulotomy. Participants also received the routine postoperative treatment prescribed for both study groups.
Participants underwent Nd:YAG laser posterior capsulotomy without receiving prophylactic timolol maleate. Intraocular pressure was measured before the procedure and 1 hour after capsulotomy. Participants received the same routine postoperative treatment as the experimental group.
Multan, Punjab Province 66000, Pakistan
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