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A study to assess the safety of the Helix Surgical System in cataract surgery and to gain early evidence of its effectiveness in lowering intraocular pressure (IOP) in subjects with mild to moderate primary open-angle glaucoma (POAG) and cataracts.
To assess the safety of the Helix Surgical System with cataract surgery and gain early evidence on intraocular pressure (IOP) -lowering effectiveness in subjects with mild-moderate primary open-angle glaucoma (POAG) and cataract.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| POAG and Cataracts | Experimental | Subjects diagnosed with mild to moderate primary open angle glaucoma (POAG) and cataracts in the study eye. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Helix Surgical System | Device | A handheld device to viscodilate up to 360 degrees of Schlemm's canal and collector channels that also enables intracanalicular scaffolding procedure to restore the aqueous outflow system of a glaucomatous eye. |
| Measure | Description | Time Frame |
|---|---|---|
| ≥ 20% change from baseline in mean IOP at the 3-month post-operative endpoint | Proportion of subjects with a ≥ 20% change from baseline in mean IOP at the 3-month post-operative endpoint and on the same or fewer medications as preoperatively. | 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Change in mean IOP | Change in mean IOP at 3 months post-operatively | 3 months |
| Average number of ocular hypotensive medications | Average number of ocular hypotensive medications used at 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of ocular adverse events (AE) | Rate of intraoperative and postoperative ocular adverse events (AE) | 3 months |
Inclusion Criteria:
Exclusion Criteria:
Any of the following prior ocular procedures:
Laser trabeculoplasty ≤180 days prior to baseline
Durysta ≤12 months prior to baseline
Any implanted glaucoma device
Prior canaloplasty, goniotomy, trabeculotomy, trabeculectomy
Ciliary ablation including endoscopic cyclophotocoagulation (ECP), Cyclophotocoagulation or CPC (G probe), high intensity focused ultrasound (HIFU),
Retinal laser procedure ≤3 months prior to baseline
Any form of glaucoma other than POAG
Use of topical ocular steroids.
Clinically significant concurrent ocular pathology or systemic medical condition which, in the Investigator's judgment, would either place the subject at increased risk of complications, contraindicate surgery, place the subject at risk of significant vision loss during the study period or interfere with compliance to elements of the study protocol
History of penetrating keratoplasty or another corneal transplant
Endothelial cell density < 2200 cells/mm2 (age 45), < 2000 cells/mm2 (age 46 to 55), < 1800 cells/mm2 (age 56 to 65), < 1600 cells/mm2 (age > 65).
Retrobulbar tumor, thyroid eye disease, Sturge-Weber Syndrome or any other type of condition that may cause elevated episcleral venous pressure.
BCVA of logMAR 0.4 (20/50) or worse in the study eye not due to cataract
BCVA of logMAR 0.6 (20/80) or worse in the non-study eye not due to cataract.
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| Name | Affiliation | Role |
|---|---|---|
| Jaime Dickerson, PhD | Sight Sciences, Inc. | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Panama Eye Center | Panama City | Panama |
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| ID | Term |
|---|---|
| D005902 | Glaucoma, Open-Angle |
| D002386 | Cataract |
| ID | Term |
|---|---|
| D005901 | Glaucoma |
| D009798 | Ocular Hypertension |
| D005128 | Eye Diseases |
| D007905 | Lens Diseases |
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Prospective, single-center, single-arm, clinical trial
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| 3 months |