Clinical Trials Logo

Clinical Trial Summary

Newborn and children can be affected by two subgroups of this disease: (1) primary congenital glaucoma (PCG) or (2) developmental glaucoma (DG). The primary aim of this study is to compare the Santen PRESERFLO implant to trabeculectomy in PCG and DG patients as second surgery after failed trabeculotomy or goniotomy.


Clinical Trial Description

Glaucoma is a chronic, progressive disease, leading to blindness if untreated or insufficiently treated. It is characterized by a loss of optic nerve fiber and a glaucomatous optic disc excavation and, a corresponding pattern of visual field loss. Newborn and children can be affected by two subgroups of this disease: (1) primary congenital glaucoma (PCG) or (2) developmental glaucoma (DG). PCG and DG are treated surgically, either by goniotomy or by trabeculotomy as first approach, and not with topical hypotensive medications. Whenever these procedures have failed, the subsequent surgical procedure is usually trabeculectomy with Mitomycin C or the implantation of a glaucoma drainage device. However, there is a lack of evidence regarding the "optimal" surgical approach after failed goniotomy/trabeculotomy. Optimal treatment in this young group of patients with a long life expectancy is crucial to prevent blindness, allow them to participate in a "normal" school and work environment, and to minimize disease burdens for these patients and their families as well as to minimize costs for society. Consequently, there is the desire to find a procedure with a superior success rate and even fewer or less severe complications compared to trabeculectomy. Recently, the Santen PRESERFLO was introduced. The results proved fewer complications and comparable efficacy to trabeculectomy, according results presented at scientific meetings. Yet, there are no published studies to compare the both procedures. The primary aim of this study is to compare the Santen PRESERFLO implant to trabeculectomy in PCG and DG patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04647929
Study type Interventional
Source University of Zurich
Contact
Status Withdrawn
Phase N/A
Start date December 1, 2020
Completion date June 1, 2023

See also
  Status Clinical Trial Phase
Recruiting NCT01020721 - The Genetic Characteristics in South Korean Patients With Primary Congenital Glaucoma N/A
Not yet recruiting NCT04709497 - Surgery for Primary Congenital Glaucoma in Neonates N/A
Completed NCT04116450 - MicrocatheterTrabeculotomy in Primary Congenital Glaucoma N/A
Completed NCT03541551 - Ologen® Collagen Matrix in Patients With Primary Congenital Glaucoma Undergoing Trabeculectomy N/A
Recruiting NCT04949555 - Long Term Evaluation of Primary Congenital Glaucoma Management in Sohag University Hospital
Completed NCT04683289 - Visco-Circumferential-Suture-Trabeculotomy Versus Trabeculotomy N/A
Not yet recruiting NCT05205122 - Evaluation of Primary Congenital Glaucoma at Asyut University Hospital N/A
Not yet recruiting NCT04079725 - Iris Tissue in Primary Congenital Glaucoma N/A