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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03321253
Other study ID # 2011-KAEK-2 2017/172
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 23, 2015
Est. completion date May 16, 2016

Study information

Verified date July 2019
Source Afyon Kocatepe University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It has been hypothesized that potential effects of laser Nd: YAG laser posterior capsulotomy may affect macular pigment as well as choroidal thickness, macular thickness and anterior chamber parameters, so it was aimed to investigate possible effects of Nd: YAG laser posterior capsulotomy on macular pigment optical density, choroidal thickness, macular thickness and anterior chamber parameters in cases with posterior capsule opacification in this study.


Description:

This clinical trial was conducted following the principles of the Declaration of Helsinki. The local authorized clinical trials ethics committee approved the protocol and consent forms (Afyon Kocatepe University Clinical Trials Ethics Committee, 2011-KAEK-2 2017/172). Between 2015 and 2016, 38 pseudophakic participants were enrolled in this study. After providing information to patients about the disease and treatment, patients predicted to show adherence to treatment, were enrolled in the study.

Detailed ophthalmological examinations of all subjects were performed prior to Nd: YAG laser posterior capsulotomy intervention. Anterior chamber parameters of cases with PCO were measured Measurements of IOP, anterior chamber parameters, visual acuity, Slit-lamp, gonioscopy and fundus examinations, and measurements of central macular thickness (CMT), choroidal thicknesses (CTs), and MPOD were performed after maximal pupil dilatation.

Proposed procedure, including risks, benefits, and alternatives were discussed with all subjects, and all participants signed of informed consent form.

Choroidal thicknesses were recorded as subfoveal CT (SCT), nasal CT (NCT) and temporal CT (TCT).

MPOD measurements were subsequently made by using luminance differential thresholds test. After measurements a refractive surgery specialist carried out Nd: YAG laser posterior capsulotomy interventions to patients who were decided to applying Nd:YAG laser capsulotomy.

All examinations and measurements were repeated and recorded at 1st week, 1st and 2nd month.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date May 16, 2016
Est. primary completion date April 12, 2016
Accepts healthy volunteers No
Gender All
Age group 45 Years to 65 Years
Eligibility Inclusion Criteria:

- Best-corrected visual acuity (BCVA) logMAR <0.3

- Duration at least 2 years after cataract surgery

- Between the ages of 45 and 65 years (45=age=65)

Exclusion Criteria:

- Corneal scarring, diffuse posterior PCO or intravitreal hemorrhage that prevents appearance of the fundus

- Occluded angle by gonioscopy (grade 0, narrow angle, grade I, grade II)

- Presence of macular or peripheral retinal pathologies or choroidopathy

- High risk for RD

- Presence of macular edema in the macular area

- Detection of macular fluid or edema in OCT

- Active intraocular inflammation

- Previous laser PRP, Nd: YAG laser posterior capsulotomy, laser iridotomy or selective laser trabeculoplasty interventions

- Previous iridectomy, glaucoma or vitreoretinal surgery

- Glass intraocular lens

- Spherical refractive error = ±6.00 D or cylinder refractive error = ±3.00 D

- Inadequate stability of the eye

- Systemic diseases that may affect the choroidal blood flow such as cardiological diseases

- Current use of carotenoid supplementation

- Changing eating habits

- Gastrointestinal diseases that could cause disturbance of dietary absorption

Study Design


Intervention

Device:
Nd: YAG laser posterior capsulotomy
Nd: YAG laser posterior capsulotomy

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Afyon Kocatepe University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Changes of Foveal and Pericentral Pigment Optical Density (Log Unit) From Baseline at 2 Months Foveal and pericentral pigment optical density was measured by using color perimetry technique and recorded as log unit before Nd: YAG laser posterior capsulotomy, at 1 week, 1 month and 2 months 2 months
Primary Changes of Subfoveal, Temporal and Nasal Choroidal Thicknesses (Micrometer) From Baseline at 2 Months Subfoveal, temporal and nasal choroidal thicknesses were measured by using enhanced-deep imaging optical coherence tomography and recorded as micrometer before Nd: YAG laser posterior capsulotomy, at 1 week, at 1-month and at 2-month 2 months
Primary Changes of Anterior Chamber Depth (Millimeter) From Baseline at 2 Months Anterior chamber depth was measured by using anterior segment module optical coherence tomography and recorded as millimeter before Nd: YAG laser posterior capsulotomy, at 1 week, at 1-month and at 2-month 2 months
Primary Changes of Iridocorneal Angle From Baseline at 2 Months Iridocorneal angle was measured by using anterior segment module optical coherence tomography and recorded as millimeter before Nd: YAG laser posterior capsulotomy, at 1 week, at 1-month and 2-month 2 months
Secondary Changes of Central Macular Thicknesses (Micrometer) From Baseline at 2 Months 2 Months
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