NCT05446077

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
129

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2020

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2020

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2021

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

June 26, 2022

Completed
10 days until next milestone

First Posted

Study publicly available on registry

July 6, 2022

Completed
Last Updated

July 6, 2022

Status Verified

July 1, 2022

Enrollment Period

3 months

First QC Date

June 26, 2022

Last Update Submit

July 3, 2022

Conditions

Outcome Measures

Primary Outcomes (3)

  • 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

  • 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

  • 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

Eligibility Criteria

Age4 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodProbability Sample
Study Population

This study is a cross-sectional clinical study. Including children who were followed up in the pediatric cataract clinic of our hospital from December 1, 2020, to March 31, 2021, and had been diagnosed with GFCS, as well as patients diagnosed with non-congenital cataract extraction after surgery(NGFCS).

You may qualify if:

  • \) The guardian of the child voluntarily signed the informed consent;
  • \) 4 years old ≤ age ≤ 18 years old, regardless of gender;
  • \) 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;
  • \) No other serious postoperative complications other than GFCS occurred after cataract extraction, such as retinal detachment, vitreous hemorrhage, choroidal detachment, etc.
  • \) 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;
  • \) The guardian of the child voluntarily signed the informed consent;
  • \) Clinical diagnosis of GFCS
  • \) The age of 4 years old is less than or equal to 18 years old, and the gender is not limited;
  • \) 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
  • Intraocular pressure: \>21 mmHg (investigator discretion on method of measurement and if EUA data alone is sufficient).
  • Visual fields: reproducible visual field defect that is consistent with glaucomatous optic neuropathy with no other observable reason for the visual field defect.
  • Axial length: progressive myopia or myopic shift with increased ocular dimensions that outpace normal growth.
  • 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.
  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Zhongshan Ophthalmic Center

Guangzhou, Guangdong, 510000, China

Location

Study Officials

  • Haotian Lin

    Zhongshan Ophthalmic Center, Sun Yat-sen University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Target Duration
4 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

June 26, 2022

First Posted

July 6, 2022

Study Start

December 1, 2020

Primary Completion

March 1, 2021

Study Completion

March 1, 2021

Last Updated

July 6, 2022

Record last verified: 2022-07

Locations