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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04648943
Other study ID # ES8/Th11/10-10-2013
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2013
Est. completion date November 30, 2016

Study information

Verified date November 2020
Source Democritus University of Thrace
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to look into the change of the corneal biomechanical properties in patients undergoing insertion of the Ex-PRESS mini shunt or trabeculectomy for medically uncontrolled glaucoma


Description:

The patients in the study were divided into two groups. In group 1 the patients had the Ex-PRESS mini shunt inserted in the operated eye and in group 2 the patients underwent standard trabeculectomy. The corneal biomechanical properties were measured with the Ocular Response Analyzer before surgery and at 1, 6 and 12 months after surgery. The corneal biomechanical properties measured were the Corneal Hysteresis (CH) and the Corneal Resistance Factor (CRF). The change of the CH and CRF was compared in each group before and after surgery (at the aforementioned predetermined time points) and between the two groups. The intraocular pressure was also measured with the Goldmann applanation tonometer at the same time points and the change was compared before and after surgery in each group and between the two groups.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date November 30, 2016
Est. primary completion date May 31, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age > 18 - Average Intraocular pressure > 24 mmHg on at least 2 occasions 1 month before surgery - Congenital glaucoma Exclusion Criteria: - Previous ocular trauma - Previous ocular surgery other than phacoemulsification - Previous disease of the ocular surface

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Ex-Press mini shunt insertion

Trabeculectomy


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Democritus University of Thrace

Outcome

Type Measure Description Time frame Safety issue
Primary Change of corneal biomechanical properties Two corneal biomechanical properties were measured with the use of the Ocular Response Analyzer (ORA): the Corneal Resistance Factor (CRF) and the Corneal Hysteresis (CH).
These two indicators were measured before surgery and at 1, 6 and 12 months after surgery
12 months
Secondary Change of Intraocular Pressure The Intraocular Pressure was measured with the Goldmann applanation tonometer before surgery and at 1, 6 and 12 months after surgery 12 months
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