Clinical Trials Directory

Trials / Completed

CompletedNCT06237764

Genetic and Risk Factors in Exfoliation Glaucoma Patients

Genetic and Risk Factors in Exfoliation Glaucoma Patients in Sweden

Status
Completed
Phase
Study type
Observational
Enrollment
130 (actual)
Sponsor
Göteborg University · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Prospective non-randomised cohort study enrolling patients with exfoliation glaucoma. All patients were ophthalmological examined at inclusion. Blood samples were taken for genetic analysis.

Detailed description

Patients \& examinations In this prospective non-randomised cohort study, the investigators enrolled patients with exfoliation glaucoma at the Ophthalmology Department of the Skaraborg's Hospital, Skövde, and Sahlgrenska University Hospital, Gothenburg, from 1st January, 2014, to 31st December, 2017. All patients were followed-up for three years ± three months. Informed consent was obtained from all patients. The study protocol was granted ethical approval by the University of Gothenburg (DN:119-12). The study was performed in accordance with the tenets of the Declaration of Helsinki. At the recruiting visit, an ophthalmic nurse checked the visual acuity of patients with a Snellen's chart and performed a visual field test. Humphrey Field Analysis was performed using the software threshold 24-2. Subsequently, an ophthalmologist measured the intracoular pressure (IOP) with a Goldmann applanation tonometer and performed slit-lamp biomicroscopy, including gonioscopy. Pupils were then dilated with 2.5% phenylephrine and 0.5% tropicamide. After 20 min, the presence of exfoliation was confirmed, and the optic nerve was assessed using a 90-D lens. Subsequently, the central corneal thickness (CCT) was measured using an ultrasound device. The average value of seven measurements was automatically calculated. At the end of the visit, blood samples were collected. The number of medicines was registered as the number of compounds and not the number of bottles used.

Conditions

Interventions

TypeNameDescription
OTHERNo interventionNo intervention.

Timeline

Start date
2014-01-01
Primary completion
2017-12-31
Completion
2019-01-01
First posted
2024-02-01
Last updated
2024-02-01

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT06237764. Inclusion in this directory is not an endorsement.