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The study objective was to evaluate the efficacy and safety of transscleral cyclophotocoagulation (TSCPC) using micropulse diode laser treatment in patients with various types of glaucoma.
Evaluation of the efficacy and safety of a new form of transscleral cyclophotocoagulation (TSCPC) using micropulse diode laser treatment in patients with various types of glaucoma.
In this study, 810 nm infrared diode laser radiation in the micro- pulse mode was used in conjunction with a G probe (IRIDEX Medical Instruments, Mountain View, CA, USA).
The laser settings ranged from 2000- 2500 mW of 810 nm infrared diode laser set on micro- pulse mode, delivered over 100-200 seconds (envelope of micropulses) depending on severity of the case and other patient factors. With duty cycle 31.3% (This translates to 0.5 ms "on" time and 1.1 ms "off" time), which allows the tissue to cool down between laser shots, thus greatly reducing thermal damage.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Glaucoma patients | Other | Patients were enrolled from outpatient clinic with glaucoma during the period between January 2020 and July 2021 |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Micropulse transscleral cyclophotocoagulation (MP-TSCPC) | Device | patients undergone micropulse laser transscleral cyclophotocoagulation. The laser settings ranged from 2000- 2500 mW of 810 nm infrared diode laser radiation set on micro- pulse mode (Iris Medical Instruments, Mountain View, CA, USA), delivered over 100-200 s (envelope of micropulses) depending on severity of the case and other patient factors. Follow-up was done at day 1, week 1, month 1, month 3, and month 6 postoperatively. |
| Measure | Description | Time Frame |
|---|---|---|
| Intraocular pressure (IOP) | significant change in IOP in mmHg. | Follow-up was done at day 1, week 1, month 1, month 3, and month 6 postoperatively |
| best corrected visual acuity (BCVA) | change in BCVA using snellen's chart | Follow-up was done at day 1, week 1, month 1, month 3, and month 6 postoperatively |
| Measure | Description | Time Frame |
|---|---|---|
| complication rate. | Describing any complications related to the procedure. | Follow-up was done at day 1, week 1, month 1, month 3, and month 6 postoperatively |
| change in number of postoperative glaucoma medications. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Gehad H Youssef, Msc | Benha University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Benha University | Banhā | Other | 13511 | Egypt |
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| ID | Term |
|---|---|
| D005901 | Glaucoma |
| ID | Term |
|---|---|
| D009798 | Ocular Hypertension |
| D005128 | Eye Diseases |
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|
Number of postoperative glaucoma medications.
| Follow-up was done at day 1, week 1, month 1, month 3, and month 6 postoperatively |
| retreatment rate. | percentage of patients needing further treatment. | Follow-up was done at day 1, week 1, month 1, month 3, and month 6 postoperatively |