Angle Closure (Glaucoma) in Caucasians

Glaucoma, Angle-Closure Clinical Trial

Official title:

Structural and Functional Parameters in Caucasian Patients With Angle Closure on SS-OCT

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT02054403
• Other study ID #: NL47347.068.13/METC 13-2-060
• Status: Not yet recruiting
• Phase: N/A
• First received: January 30, 2014
• Last updated: February 3, 2014
• Start date: April 2014
• Est. completion date: October 2015

Study information

• Verified date: February 2014
• Source: Maastricht University Medical Center
• Contact: Carroll AB Webers, MD, PhD, FEBOpht
• Phone: +31 43 3875346
• Email: c.webers[@]mumc.nl
• Is FDA regulated: No
• Health authority: Netherlands: Medical Ethics Review Committee (METC)
• Study type: Observational

Clinical Trial Summary

Rationale: Primary angle closure glaucoma (PACG) causes high rates of blindness, either by means of a painful attack of acute angle closure glaucoma or unnoticed over a period of many years. Patients with angle closure are particularly at risk but can be detected during an ophthalmological examination and sent for early preventive (laser) intervention. Current practice shows that patients at risk of PACG are frequently missed during routine examinations. Moreover, new imaging techniques like swept source optical coherence tomography (SS-OCT), are emerging with which the angle of the anterior chamber can be imaged in great detail with no burden for the patient. These techniques are already used in clinical practice and replace and complete part of the ophthalmic examination. However, in Caucasians, it is not yet known to what extent angle closure is detected in regular care and can be detected with this OCT device. There are few published data concerning angle closure and PACG in Caucasians and its characteristics.

Objective: To quantify the presence of angle closure by gonioscopy in patients at risk of angle closure on SS-OCT. Secondary objectives are to quantify the presence of an increased intra-ocular pressure during the day or after dark provocation, to quantify morphometric details of the anterior chamber, structural changes, and corneal endothelial cells and to quantify the functional changes of the visual field.

Study design: prospective, observational, descriptive study. Study population: Caucasian patients, presenting at the outpatient clinic of the University Eye Clinic Maastricht, aged 40 to 80 years, who are diagnosed with angle closure on SS-OCT.

Intervention (if applicable): Not applicable. Main study parameters/endpoints: The main study parameter is assessment of the anterior chamber angle according to gonioscopy. Secondary study parameters are the presence of an increased intra-ocular pressure (IOP) (>21 mmHg) during the day or after dark provocation (IOP rise from baseline), morphometric details of the anterior chamber, structural changes of the retinal nerve fiber layer, number of corneal endothelial cells and functional changes of the visual field Hypothesis: It is hypothesised that, based on its resolution and ease of use, SS-OCT is a suitable imaging technique to identify patients with or at risk of angle closure. It will be of value as an additional diagnostic instrument and may even replace gonioscopy.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: October 2015
• Est. primary completion date: April 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 40 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Caucasian race

2. 40-80 years

3. Willing and able to comply with scheduled visits and other study procedures

4. Signed informed consent

5. Participants derived from the study 'Caucasian patients with angle closure on SS-OCT' AND 1 or more of the following:

• Irido-trabecular contact (ITC) in =2 quadrants as seen with SS-OCT in darkened conditions

• Scleral spur angle (SSA) <20° (in 0 and 180º) AND anterior chamber depth (ACD) < 2.5 mm as seen with SS-OCT in darkened conditions

• The fellow, non-treated eye in a patient after an acute primary angle closure (APAC) attack in the other eye. APAC is defined as an abrupt onset of symptomatic elevation of IOP resulting from total closure of the angle which is typically not self-limiting (although acute attacks can rarely resolve spontaneously).

Exclusion Criteria:

1. Any condition including (previous) intraocular laser/incisional surgery or medical procedure or treatment in ophthalmology

2. Any eye condition/abnormality that will affect the acquisition/reliability of measurement (results), (e.g. vitreous haemorrhage, uveitis, intraocular trauma, significant corneal opacity)

3. Unable to communicate properly or to understand instructions

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Glaucoma
• Glaucoma, Angle-Closure

Locations

Country	Name	City	State
Netherlands	University Eye Clinic Maastricht	Maastricht

Sponsors (1)

Lead Sponsor	Collaborator
Maastricht University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Visual field loss	The percentage of patients with visual field loss on the HFA visual field.	3 weeks	No
Other	Retinal nerve fiber layer thickness	The mean RNFL thickness will be measured.	3 weeks	No
Other	Number of corneal endothelial cells	The mean number of corneal endothelial cells will be measured	3 weeks	No
Other	Axial length	The mean axial length will be measured.	3 weeks	No
Other	Anterior chamber angle parameters	Parameters analysed from SS-OCT images to determine the morphometric details of the anterior chamber will be measured and means will be calculated.; For example AOD500, AOD750, TISA500, TISA750, ARA500, ARA750,TIA500, TIA750, ACD, LV	3 weeks	No
Primary	Angle closure on gonioscopy	The percentage of subjects with angle closure on gonioscopy compared with angle closure on SS-OCT.	3 weeks	No
Secondary	intra-ocular pressure (IOP)	The secondary outcome measure is the percentage of patients with presence of an increased intra-ocular pressure (>21 mmHg) during the day or after dark provocation (IOP rise from baseline)	3 weeks	No