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Clinical Trials/DRKS00013987
DRKS00013987
Completed
Not Applicable

Retrospective, monocentric study for comparative analysis of postoperative results after CyPass implantation with and without bevacizumab (intracameral) for wound healing modulation - ReCyBe

Klinik für Augenheilkunde, Dietrich-Bonhoeffer-Klinikum,0 sites313 target enrollmentDecember 4, 2018
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ConditionsH40.1Primary open-angle glaucoma

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
H40.1
Sponsor
Klinik für Augenheilkunde, Dietrich-Bonhoeffer-Klinikum,
Enrollment
313
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 4, 2018
End Date
September 29, 2018
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Klinik für Augenheilkunde, Dietrich-Bonhoeffer-Klinikum,

Eligibility Criteria

Inclusion Criteria

  • •Patients with primary chronic open angle glaucoma
  • •\- Implantation of the CyPass stent at the Department of Ophthalmology at the Dietrich\-Bonhoeffer\-Klinikum Neubrandenburg between March 2009 and September 2016
  • •\- data of follow\-up visits available after 3 and 6 months
  • •\- Patient age \=18 years

Exclusion Criteria

  • •\- surgery canceled
  • •\- more than 3 hours difference in the time of pre\- and postoperative intraocular pressure measurement
  • •\- Additional exclusion criterion for the evaluation of the data concerning the effectiveness:
  • •\-\- postoperative rTPA injection

Outcomes

Primary Outcomes

Not specified

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