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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05446077
Other study ID # CCMPOH2022-01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2020
Est. completion date March 1, 2021

Study information

Verified date July 2022
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To quantitatively analyze the fundus structure and microvascular characteristics of GFCS and non-GFCS (NGFCS) using optical coherence tomography angiography (OCTA), to explore the vascular-structural association, and to assess the diagnostic abilities of structure parameters.


Description:

A cross-sectional study. A total of 129 congenital cataract patients after congenital cataract extraction (40 in GFCS and 89 in NGFCS) were enrolled in this study from December 2020 to March 2021. All participants, age range from 4 to 18 years old, completed OCT examinations (including macular structure parameters, optic nerve fiber layer thickness periphery retinal nerve fiber layer [pRNFL], and sub foveal choroidal thickness [SFCT]). All the NGFCS participants underwent OCTA examinations (including vessel density (VD) and perfusion density (PD) of macular and peripapillary area.). Linear regression models were used to examine the effect of various factors on different ocular parameters. Vascular-structural associations were assessed with Spearman correlation. Diagnostic ability was evaluated with area under the receiver operating curve (AUC).


Recruitment information / eligibility

Status Completed
Enrollment 129
Est. completion date March 1, 2021
Est. primary completion date March 1, 2021
Accepts healthy volunteers No
Gender All
Age group 4 Years to 18 Years
Eligibility NGFCS Group Inclusion Criteria: - 1) The guardian of the child voluntarily signed the informed consent; - 2) 4 years old = age = 18 years old, regardless of gender; - 3) In line with the diagnostic criteria of NGFCS; that is, cataract extraction surgery was performed in our hospital, with no restrictions on the eye of the surgery, and implantation / or no intraocular lens implantation; - 4) No other serious postoperative complications other than GFCS occurred after cataract extraction, such as retinal detachment, vitreous hemorrhage, choroidal detachment, etc. - 5) The children included in this study need to have good gaze ability. Considering that the visual acuity of CC children after cataract extraction is lower than that of normal children of the same age, the best-corrected visual acuity of the included patients is =0.4logMAR (implanted IOL or wearing frame glasses, Contact lenses to correct vision), can better cooperate to complete OCT and OCTA examinations; GFCS Group Inclusion Criteria: - 1) The guardian of the child voluntarily signed the informed consent; - 2) Clinical diagnosis of GFCS - 3) The age of 4 years old is less than or equal to 18 years old, and the gender is not limited; - 4) The diagnostic criteria of GFCS are met; one or both eyes are affected; Tremor, best corrected visual acuity =0.7logMAR, can better cooperate with OCT and OCTA examination; The diagnostic criteria of GFCS: Childhood: based on national criteria, <18 years old (USA); 16 years old (UK, Europe,UNICEF) Childhood glaucoma: two or more of the following are required 1. Intraocular pressure: >21 mmHg (investigator discretion on method of measurement and if EUA data alone is sufficient). 2. Visual fields: reproducible visual field defect that is consistent with glaucomatous optic neuropathy with no other observable reason for the visual field defect. 3. Axial length: progressive myopia or myopic shift with increased ocular dimensions that outpace normal growth. 4. Cornea: findings including Haab striae, corneal diameter >11mm in newborns, >12mm in children younger than 1 year old, and >13mm in children older than 1 year old. 5. Optic nerve: progressive increase in cup-disc ratio, cup-disc asymmetry of 0.2 when optic discs are of similar size, and focal rim thinning.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Zhongshan Ophthalmic Center Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Linear regression models were used to examine the effect of various factors on different ocular parameters with demographic factors. (RNFL thickness with gender, age, axial length) All participants completed OCT examinations (including macular structure parameters, optic nerve fiber layer thickness periphery retinal nerve fiber layer [pRNFL], and sub foveal choroidal thickness [SFCT]). All the NGFCS participants underwent OCTA examinations (including vessel density (VD) and perfusion density (PD) of macular and peripapillary area.). Linear regression models were used to examine the effect of various factors on different ocular parameters with demographic factors. December 1st 2020 to March 31st 2021
Primary Vascular-structural associations were assessed with Spearman correlation. (RNFL thickness and ONH vessels density, perfusion density) All participants completed OCT examinations (including macular structure parameters, optic nerve fiber layer thickness periphery retinal nerve fiber layer [pRNFL], and sub foveal choroidal thickness [SFCT]). All the NGFCS participants underwent OCTA examinations (including vessel density (VD) and perfusion density (PD) of macular and peripapillary area.). Vascular-structural associations were assessed with Spearman correlation. December 1st 2020 to March 31st 2021
Primary Diagnostic ability of GFCS was evaluated with area under the receiver operating curve (AUC). All participants completed OCT examinations (including macular structure parameters, optic nerve fiber layer thickness periphery retinal nerve fiber layer [pRNFL], and sub foveal choroidal thickness [SFCT]). All the NGFCS participants underwent OCTA examinations (including vessel density (VD) and perfusion density (PD) of macular and peripapillary area.). Diagnostic ability of GFCS was evaluated with area under the receiver operating curve (AUC). December 1st 2020 to March 31st 2021
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