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UnknownNCT00349414

Safety Study of Conventional Versus Micropulse Transscleral Cyclophotocoagulation in Treating End-Stage Glaucoma

A Comparison of the Safety and Efficacy of Conventional Versus Micropulse Transscleral Diode Laser Cyclophotocoagulation in Refractory Glaucoma

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
National University Hospital, Singapore · Academic / Other
Sex
All
Age
22 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to compare the safety and efficacy of conventional and micropulse transscleral diode laser in the treatment of end-stage glaucoma.

Detailed description

End-stage glaucoma is difficult to treat, and it may sometimes be unresponsive to surgery or medications. A common treatment is the conventional transscleral cyclophotocoagulaion, but it has various side effects. This study specifically aims to compare the intraocular pressure (IOP) lowering effects and the incidence of complications such as hypotony, phthisis, sympathetic ophthalmia, surface conjunctival burns, bulbar conjunctival swelling, decompensation of corneal grafts, hyphema and vitreous hemorrhage, in conventional and the newer micropulse transscleral cyclophotocoagulation.The hypothesis is that the micropulse transscleral cyclophotocoagulation will be as good or better than the conventional transscleral cyclophotocoagulation, with less complications.

Conditions

Interventions

TypeNameDescription
PROCEDUREMicropulse Transscleral Cyclophotocoagulation
PROCEDUREConventional Transscleral Cyclophotocoagulation

Timeline

Start date
2006-07-01
Completion
2008-12-01
First posted
2006-07-07
Last updated
2008-05-15

Locations

1 site across 1 country: Singapore

Source: ClinicalTrials.gov record NCT00349414. Inclusion in this directory is not an endorsement.

Safety Study of Conventional Versus Micropulse Transscleral Cyclophotocoagulation in Treating End-Stage Glaucoma (NCT00349414) · Clinical Trials Directory