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| Name | Class |
|---|---|
| Canadian Glaucoma Clinical Research Council | OTHER |
| Pfizer | INDUSTRY |
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The present study's main objective is to assess if there is a significant difference between either of the treatments frequently used in post-op, namely a topic cortisone-based treatment, an non-steroidal anti-inflammatory drug (NSAID) or simply a placebo, in order to gain the best long term (6 months) efficacy of the SLT.
The selective laser trabeculoplasty (SLT) is the laser treatment of choice for treating glaucoma. A There is however a controversy regarding the use of drops post-treatment. Indeed, some would prefer not to pharmacologically modulate the post-op inflammatory response which can be an integral part of the treatment by favouring the mobilisation of the macrophages which participate to the trabeculae "cleaning". Others will prefer to calm the inflammatory reaction and choose an anti-inflammatory drug (either steroidal or non-steroidal).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Prednisone acetate 1% | Active Comparator | A topic cortisone-based treatment |
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| diclofenac 0.1% | Active Comparator | an non-steroidal anti-inflammatory drug |
|
| Artificial Tears | Placebo Comparator | Pharmasciences DIN: 02229570 |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Selective Laser trabeculoplasty | Procedure | The Selective Laser Trabeculoplasty is done with the Latina lens after applying a drop of iopidine in the treated eye and alcaïne in both eye. Fifty spots are done over 180°. The maximal and total energy is written in the chart. After the treatment, prednisolone acetate 1% (a corticosteroid), diclofenac 0.1% (an NSAID) or a placebo is used. The three treatments were administered 4 times a day (at breakfast, lunch, dinner and at bedtime) for five days. |
| Measure | Description | Time Frame |
|---|---|---|
| Intraocular pressure in the treated eye | 1 hour, 7 days, 1.5, 3 and 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Side effects (include a slight uveitis, oculary discomfort and a spike in intraocular pressure in the immediate post-op period) | 1 hour, 7 days, 1.5 months, 3 months and 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Béatrice Des Marchais, FRCSC M.Sc. | CHU de Quebec-Universite Laval | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre universitaire d'ophtalmologie, Hôpital du Saint-Sacrement, CHU de Québec | Québec | Quebec | G1S 4L8 | Canada |
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| ID | Term |
|---|---|
| D005901 | Glaucoma |
| D009798 | Ocular Hypertension |
| ID | Term |
|---|---|
| D005128 | Eye Diseases |
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