CompletedNot Applicable

5 Years Long Term Results After Standalone CyPass-Implantation

Germany230 participantsStarted 2017-02-01

Plain-language summary

This study evaluates the results of all clinically relevant findings of glaucoma diagnostics 5 Years after stent-implantation concerning the safety and effectiveness of the cypass stent procedure. The comparison of Preoperative and long term postoperative results is the aim of this study to evaluate this young procedure of Glaucoma surgery

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * patients who have undergone a standalone cypass implantation at least 3 years ago * signed inform consent Exclusion Criteria: * Patients with too much travel distance between study center and home * Patients who cannot visit the studycenter due to health problems

What they're measuring

Number of Patients That Achieve Target Intraocular Pressure Measured in mmHg

Timeframe: up to 7 years

Change of Intraocular Pressure in mmHg Preoperatively (at Screening) vs Postoperatively (at Final Examination)

Timeframe: up to 7 years

Number of Additional Medication

Timeframe: up to 7 years

Number of Participants With Secondary Glaucoma Procedures

Timeframe: up to 7 years

Trial details

NCT IDNCT03114059

SponsorDietrich-Bonhoeffer-Klinikum

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2018-02-28

Results submitted2021-08-17

View on ClinicalTrials.gov More Glaucoma trials