Glaucoma, Progression, Surgery
Conditions
Brief summary
The trabeculectomy is the gold standard in glaucoma surgery, nevertheless often postoperative interventions have to be done. (1),(2) The PreserFlo MicroShunt (Santen, Osaka, Japan) implantation occurs without critical steps of trabeculectomy. (3) According to a study a 20% eye pressure reduction was achieved in 53.9% of patients one year after PreserFlo MicroShunt implantation and the risk of postoperative hypotony was clearly minimized. (4) It has been shown that after trabeculectomy there is a stable development of visual fields in the first 3 months after surgery and then, despite adequate intraocular pressure reduction, visual fields deteriorate. (5) At the Klinikum Klagenfurt structural and functional changes after PreserFlo MicroShunt Implantation shall be evaluated.
Interventions
DEVICEPreserFlo Microshunt
The PreserFlo MicroShunt was invented to create a minimally invasive glaucoma drainage device, that comes close to the eye pressure reduction and safety profile of the current gold standard, the trabeculectomy. Reference: Pinchuk L, Riss I, Batlle JF, Kato YP, Martin JB, Arrieta E, Palmberg P, Parrish RK 2nd, Weber BA, Kwon Y, Parel JM. The development of a micro-shunt made from poly(styrene-block-isobutylene-block-styrene) to treat glaucoma. J Biomed Mater Res B Appl Biomater. 2017 Jan;105(1):211-221. doi: 10.1002/jbm.b.33525. Epub 2015 Sep 18. PMID: 26380916; PMCID: PMC5215625.
Sponsors
Medical University of Graz
Klinikum Klagenfurt am Wörthersee
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
* Patients with insufficient eye pressure control despite IOP (intraocular pressure)-lowering therapy * Diagnosis of POAG (primary open angle glaucoma) * Diagnosis of PEG (pseudoexfoliation glaucoma) * Diagnosis of PDG (pigment dispersion glaucoma) * Diagnosis of NTG (normal tension glaucoma) * Agreement of patients to participate in the study
Exclusion criteria
* Previous glaucoma surgery * Visual acuity of Nulla Lux * Poor general condition * Pregnancy * Exudative macular degeneration
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Visual field progression (mean deviation, MD) 1 month postoperative, 3 months postoperative, 6 months and 12 months postoperative after PreserFlo MicroShunt Implantation. | Visual fields taken at baseline should be compared to visual fields 1 month postoperativ, 3 months postoperative and 1 year postoperative. | Visual fields of patients at baseline preoperative and 1 month postoperative, 3 months postoperative, 6 months postoperative and 12 months postoperative should be compared. |
| RNFL (retinal nerve fiber layer) at baseline before sugery and changes after1 month, 3 months, 6 months and 12 months postoperative after PreserFlo MicroShunt Implantation will be evaluated. | The measurement of the nerve fiber index shall be done at baseline before surgery and 1 month, 3 months, 6 months and 12 months after surgery. | The measurement of the nerve fiber will be compared at baseline before surgery to the values at 1 month, 3 months, 6 months and 12 months after surgery. |
| Intraocular pressure will be taken 1 month, 3 months, 6 months and 12 months after PreserFlo MicroShunt Implantation. | The intraocular pressure will be taken postoperative after one month, 3 months, 6 months and 12 months. | The evaluation of the intraocular pressure shall be done 1 month, 3 months, 6 months and 12 months after surgery. |
Countries
Austria
Contacts
Primary ContactCarmen Gruzei
Outcome results
None listed