The Safety and Efficacy of Direct SLT in Pseudoexfoliation Glaucoma (NCT07401290) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
The Safety and Efficacy of Direct SLT in Pseudoexfoliation Glaucoma
United States40 participantsStarted 2026-03
Plain-language summary
Prospective, multi-center, single arm, interventional study evaluating DSLT in patients with pseudoexfoliative glaucoma.
Who can participate
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Inclusion Criteria:
* Adult patients diagnosed with pseudoexfoliation glaucoma (PXFG), with optic neuropathy consistent with glaucomatous damage of any severity
* Open iridocorneal angle by gonioscopy, defined as a Shafer Grade II or greater
* Treatment naive, or washed out IOP ranging from ≥18-35 mmHg
* Able to complete medication washout safely and all follow-up visits
* Participants must have a best correct visual acuity of 20/40 or better in the study eye(s), be able to undertake a reliable Humphrey visual field (HVF) (defined as fixation losses, false positives and false negatives less than 33%), and must have field loss no worse than -20 dB in treatment eye
Exclusion Criteria:
* Any contraindication to SLT or unable to have DSLT
* Angle closure glaucoma or any other types of glaucoma other than PXFG
* Prior incisional glaucoma surgery or glaucoma-related procedures in the study eye
* Any prior refractive surgery
* H/o LPI within last 6 months
* A history of any significant cataract required during study duration or cataract surgery in the last 6 months
* Prior laser trabeculoplasty (ALT/SLT)
* History of ocular inflammation and infection
* Patients who are pregnant or have any clinically relevant systemic disease that may prevent them from reliably completing follow-up visits
* Vulnerable populations that cannot provide proper informed consent will not be enrolled, such as children, prisoners, handicapped, or mentally disabled persons, or economically or educationall…