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Pseudo Exfoliation Syndrome clinical trials

View clinical trials related to Pseudo Exfoliation Syndrome.

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NCT ID: NCT06154330 Recruiting - Clinical trials for Glaucoma, Open-Angle

Safety and Efficacy of Suprachoroidal Tube Shunt in Patients With Primary Open and Pseudoexfoliation Glaucomas

Start date: November 20, 2023
Phase:
Study type: Observational

To assess safety and efficacy of a novel suprachoroidal silicone tube (SST) shunt for the treatment of primary open angle and exfoliative glaucomas.

NCT ID: NCT04911387 Completed - Glaucoma Clinical Trials

iCare® Home vs Goldmann Applanation Tonometry

Start date: April 1, 2020
Phase:
Study type: Observational

Self-tonometry with iCare Home is regularly performed at Sankt Erik's Eye Hospital since a few years back. The purpose of this study was to show that the eye pressure measurements made with iCare® Home by patients / relatives do not vary more than those made with the standard method, Goldman applanation tonometry (GAT), by different healthcare professionals. This will hopefully confirm the usefulness of self-tonometry.

NCT ID: NCT03445806 Terminated - Clinical trials for Glaucoma, Open-Angle

IOP Monitoring After Trabeculectomy Using iCare Home

Start date: February 26, 2018
Phase:
Study type: Observational

The purpose of this study is to investigate how much trabeculectomy influences intraocular pressure (IOP) fluctuations measured with iCare Home rebound tonometry (RTHome) in patients with primary open-angle glaucoma (POAG) or pseudo-exfoliation glaucoma (PEX).

NCT ID: NCT03310788 Recruiting - Clinical trials for Glaucoma Open-Angle Primary

Monitoring of the IOP After SLT Using iCare Home

Start date: October 3, 2017
Phase:
Study type: Observational

The purpose of this study is to investigate how much selective trabeculoplasty (SLT) influences intraocular pressure (IOP) fluctuations measured with iCare Home rebound tonometry (RTHome) in patients with primary open-angle glaucoma (POAG) or pseudo-exfoliation glaucoma (PEX).

NCT ID: NCT01255995 Active, not recruiting - Clinical trials for Pseudo Exfoliation Syndrome

Natural History of IOL in Pseudo Exfoliation Syndrome

PXF
Start date: December 2010
Phase: N/A
Study type: Observational

- The purpose of this study is to determine the natural course of IOL in PXF, - To demonstrate use of a clinical grading system for PXF, - To strategize a way to prevent IOL dislocation, subluxation post operatively, - To demonstrate intraoperative and long-term post-operative complications associated with phaco and PXF - To suggest evidence-based ways to minimize these complications, by using capsular tension rings (CTR), specific IOL material or size