Prophylactic Use of Timolol Maleate to Prevent Intraocular Pressure Elevation After Nd:YAG Laser Posterior Capsulotomy
NCT07729189 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 210
Last updated 2026-07-27
Summary
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.
Conditions
- Capsule Opacification
- Ocular Hypertension
Interventions
- DRUG
-
Timolol Maleate
One drop of 0.5% timolol maleate ophthalmic solution was administered topically immediately before Nd:YAG laser posterior capsulotomy.
- DRUG
-
No intervention
No prophylactic intraocular pressure-lowering medication was administered before Nd:YAG laser posterior capsulotomy.
Sponsors & Collaborators
-
CMH Multan Institute of Medical Sciences
lead OTHER_GOV
Principal Investigators
-
Ifrah Idress Lodhi · CMH Institute of Medical Sciences
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-03-10
- Primary Completion
- 2025-09-10
- Completion
- 2025-09-10
Countries
- Pakistan
Study Locations
More Related Trials
-
A Comparison of Prostaglandin E2 (PGE2) Inhibition of Acuvail(Ketorolac 0.45%), Xibrom (Bromfenac 0.09%)and Nevanac (Nepafenac)in Patients Undergoing Phacoemulsification
NCT01021761 ·Status: COMPLETED ·Phase: PHASE4
-
Comparison Between Low-Dose and High-Dose Nepafenac Sodium
NCT07749027 ·Status: COMPLETED ·Phase: NA
-
Aqueous Concentrations and PGE2 Inhibition of Ketorolac 0.4% vs. Bromfenac 0.09% in Cataract Patients: Trough Drug Effects
NCT00469690 ·Status: COMPLETED ·Phase: PHASE4
-
Corneal Protect Used During Cataract Surgery
NCT02363530 ·Status: UNKNOWN ·Phase: NA
-
Subfoveal Choroidal Thickness After Surgery for Age-related Cataracts
NCT02895074 ·Status: COMPLETED ·Phase: NA
-
Effect of Intravenous Mannitol on Anterior Chamber Depth and Intraocular Pressure.
NCT07605260 ·Status: COMPLETED ·Phase: NA
-
Steroids Versus Non-steroidal Anti-inflammatory Drugs Following Glaucoma Surgery
NCT00956462 ·Status: UNKNOWN ·Phase: NA
-
Effect of Single Incision Versus Three Planned Incisions to Reduce Pre-operative Astigmatism After Phacoemulsification.
NCT05457348 ·Status: UNKNOWN ·Phase: NA
-
Posterior Capsule Opacification Study
NCT00312299 ·Status: COMPLETED ·Phase: PHASE4
-
Dropless™ vs. Less Drops™ Pharmaceutical Regimens After Cataract Surgery
NCT02819908 ·Status: COMPLETED ·Phase: PHASE4
-
Effect of Preoperative Topical Ketorolac on Aqueous Cytokine Levels and Macular Thickness in Cataract Surgery Patients
NCT02646072 ·Status: COMPLETED ·Phase: PHASE4
-
Pharmacokinetics of the Brimonidine Tartrate Posterior Segment Delivery System in Patients Undergoing Pars Plana Vitrectomy
NCT01229410 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Compare Ocular Safety and Tolerability of Eye Drops Containing Prednisolone Acetate in Patients With Intraocular Inflammation After Cataract Surgery
NCT00170729 ·Status: COMPLETED ·Phase: PHASE4
-
Lubricating Eye Drops After Routine Cataract Surgery
NCT04465071 ·Status: COMPLETED ·Phase: NA
-
Comparing Single Versus Multiple Anti-VEGF Injections in Diabetic Patients Undergoing Cataract Surgery
NCT07301775 ·Status: NOT_YET_RECRUITING ·Phase: PHASE4
-
Effect of Prophylactic Ketorolac on CME After Cataract Surgery
NCT00335439 ·Status: COMPLETED ·Phase: NA
-
Dispervise Ophthalmic Viscoelastic as an Agent to Ensure Watertight Wound Closure After Clear Corneal Cataract Incisions
NCT01298973 ·Status: COMPLETED ·Phase: PHASE4
-
A Study of Sodium Carboxymethylcellulose for Post Cataract Surgery Dry Eye Symptoms
NCT02028754 ·Status: COMPLETED ·Phase: PHASE4
-
No Drop Post-Op Cataract Surgery
NCT03864133 ·Status: COMPLETED ·Phase: PHASE4
-
Impact of 0.1% and 0.2% Sodium Hyaluronate on Postoperative Discomfort Following Phacoemulsification Surgery
NCT03705949 ·Status: COMPLETED ·Phase: NA
-
Clinical Research of Femtosecond Laser-Assisted Cataract Surgery
NCT02492659 ·Status: COMPLETED ·Phase: NA
-
IOP Lowering Effects of Topical Anesthetics Used Frequently in the Ophthalmology Clinic
NCT01254149 ·Status: COMPLETED
-
Use of Prophylactic Lubricating Drops After Cataract Surgery
NCT04131335 ·Status: UNKNOWN ·Phase: NA
-
Femtosecond Laser for Cataract Surgery
NCT02110212 ·Status: TERMINATED ·Phase: PHASE3
-
Low-level Light Therapy Versus Intense Pulsed Light to Prevent Iatrogenic Dry Eye Disease After Cataract Surgery
NCT07055022 ·Status: NOT_YET_RECRUITING ·Phase: NA