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CompletedNCT01950832Updated Sep 26, 2013

Eye Evaluation in Patients With PCOS

An observational study in PCOS, sponsored by Gökhan Açmaz. Completed at 1 site in Turkey. Open to female participants aged 16 Years to 43 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-09-26.

Sponsored by Gökhan Açmaz · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
124
Ages
16 Years to 43 Years
Sex
Female
01

Study summary

To evaluate the macular, retinal nerve fiber layer (RNFL) and choroidal thickness alterations by using spectral-domain optical coherence tomography (SD-OCT) in polycystic ovary syndrome (PCOS) and to compare them with healthy reproductive-age women controls.

Read the detailed description

PCOS was diagnosed according to Rotterdam criteria that include (i) oligomenorrhea (interval between periods was ≥35 days) or amenorrhea (absence of vaginal bleeding for 6 months); (ii) hyperandrogenism; (iii) polycystic ovaries and exclusion of other PCOS-like syndromes, such as adrenal dysfunction, Cushing's syndrome, congenital adrenal hyperplasia, androgen-secreting tumors, enzyme deficiency (21-hydroxylase in particular), hyperprolactinemia, and thyroid dysfunction. Ultrasonographic diagnosis of polycystic ovaries was based on the presence of multiple cysts (≥12 small follicles in each ovary [2-9 mm in diameter]) arranged peripherally and scattered throughout the dense core of stroma (the necklace appearance of follicular cysts), and/or increased ovarian volume >10 ml on pelvic or vaginal ultrasound examination.

Patients who were allocated in control group had regular menstrual cycle and normal ovarian morphology detected by ultrasounds. None of the participants in both groups were pregnant. All patients were evaluated in follicular phase of their menstrual cycle.

Each subject underwent a comprehensive ophthalmologic examination. Following this detailed ophthalmologic examination, the third-generation Spectralis OCT device was used for the assessment. The OCT assessments of involved in the study were performed by the same experienced technician. The procedure was achieved without pupillary dilatation and under the same intensity of dim room lighting.

Macular thickness was determined automatically and was analyzed by OCT software. Fast Macular Thickness Map option was utilized for the macular measurements. During the assessments, macular thickness and volume analysis were used. We selected the macular map analysis protocol on the Spectralis to display numeric averages of the measurements for each of the 9 subfields as defined by the Early Treatment Diabetic Retinopathy Study (ETDRS) The peripapillary RNFL thickness parameters that were automatically calculated by the fast RNFL mode and divided into regions included temporal quadrant thickness, temporal superior quadrant thickness, nasal superior quadrant thickness, nasal quadrant thickness, nasal inferior quadrant thickness, temporal inferior quadrant thickness, and average thickness.

The method of obtaining enhanced depth imaging (EDI) OCT images has been reported previously. The resultant images were viewed and measured with the contained Heidelberg Eye Explorer software. Choroid imaging was obtained by activating the EDI button. The choroid was manually measured from the outer border of the hyperreflective line corresponding to the retinal pigment epithelium to the inner surface of the sclera. The measurements of subfoveal choroidal thickness were done by one of the authors in a masked fashion without knowledge of subject information.

02

Conditions studied

  • PCOS

Keywords

  • Structure of Retina
  • Macular Thickness
  • Retinal Nerve Fiber Layer
  • Choroidal Thickness
  • PCOS
  • Optical Coherence Tomography
03

In context

Lead sponsor

Gökhan Açmaz is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 43 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Participants:

Patients who were diagnosed with PCOS according to 2003 Rotterdam Criteria, had no physical disease but PCOS, did not receive any treatment for 6 months prior to the study for PCOS or co-morbidities and had at least primary school degre will enroll into the study. The second group consisted of 60 healthy volunteer participants in reproductive age.

Inclusion criteria

Patients who were diagnosed as PCOS according to 2003 Rotterdam Criteria, had no physical disease but PCOS, did not receive any treatment for 6 months prior to the study for PCOS or for co-morbidities and had at least primary school degree.

Exclusion criteria

Exclusion Criteria:

Patients who had thyroid disorders, hypertension, thromboembolic disease, diabetes mellitus, cardiovascular events, Cushing' disease, positive malignancy, congenital adrenal hyperplasia, liver disease,psychotic disorders and used antidepressants or steroidal hormone drugs and mood stabilizers (Li, Valproic acid, COCs, antiandrogens or insulin sensitizers etc.)

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
124 participants (actual)
Target follow-up
1 Month
Patient registry
Yes

Groups and cohorts

  • polycystic ovary syndrome (PCOS) group

    Patients who were diagnosed as PCOS according to 2003 Rotterdam Criteria.

    Other: Investigating clinically normal patients with optic coherence tomography

  • Control

    60 healthy volunteers

    Other: Investigating clinically normal patients with optic coherence tomography

Interventions

  • OtherInvestigating clinically normal patients with optic coherence tomography

    Also known as: Control Group

06

What researchers measure

Primary outcomes

  1. Macula, Retinal nerve fiber and choroid layer measurements

    Each subject underwent a comprehensive ophthalmologic examination. Following this detailed ophthalmologic examination, the third-generation Spectralis OCT device (software version 5.6.3.0; Spectralis OCT Heidelberg Engineering, Dossenheim, Germany) was used for the assessment. The OCT assessments of involved in the study were performed by the same experienced technician. The procedure was achieved without pupillary dilatation and under the same intensity of dim room lighting.

    Time frame: 1 month

Secondary outcomes

  1. Macular thickness and volume

    Central subfield, inferior inner macula, inferior outer macula, nasal inner macula, nasal outer macula, superior inner macula, superior outer macula, temporal inner macula, temporal outer maculas both thickness and volumes were evaluated.

    Time frame: 1 month

Other outcomes

  1. Retinal nerve fiber layer and choroid measurements.

    Temporal Superior, nasal Superior, nasal, nasal Inferior, temporal inferior parts of RNFL were evaluated

    Time frame: 1 month

07

Study locations

1 site
  • Kayseri Education and Research Hospital
    Kayseri, 38039, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 26, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01950832
Lead sponsor
Gökhan Açmaz
Responsible party
Gökhan Açmaz (MD, Kayseri Education and Research Hospital) — Sponsor-investigator
First posted
Sep 26, 2013
Start date
Mar 2013
Primary completion
Aug 2013
Completion
Aug 2013
Last update
Sep 26, 2013

Study contacts

Gökhan Açmaz, MD
principal investigator · Kayseri Education and Research Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2013. You cannot join it, but the record below documents what was studied.

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