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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04131114
Other study ID # CCPMOH2016-China-0303
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2011
Est. completion date December 2021

Study information

Verified date April 2020
Source Sun Yat-sen University
Contact Haotian Lin, Ph.D
Phone +86-020-87333271
Email gddlht@aliyun.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pediatric patients who have undergone surgery for congenital or infantile cataracts have a risk of developing suspected glaucoma and glaucoma, but the current evidence does not address our understanding of the incidence and associated risk factors of suspected glaucoma/glaucoma for application in clinical standard care. Therefore, this study investigated the incidence of and risk factors for suspected glaucoma/glaucoma in patients who have undergone surgery for congenital/infantile cataracts.


Description:

A prospective longitudinal cohort study of pediatric patients who underwent surgery for congenital/infantile cataracts between January 2011 and December 2021 was performed.


Recruitment information / eligibility

Status Recruiting
Enrollment 241
Est. completion date December 2021
Est. primary completion date December 30, 2019
Accepts healthy volunteers No
Gender All
Age group N/A to 10 Years
Eligibility Inclusion Criteria:

- a diagnosis of congenital/infantile cataracts without any surgical intervention;

- age younger than 10 years;

- cataract surgery performed at the Zhongshan Ophthalmic Center after enrollment

Exclusion Criteria:

- a preoperative IOP above 21 mm Hg;

- the presence of any preoperative sign of glaucoma, such as corneal enlargement, corneal clouding, excessive optic nerve cupping, or a family history of glaucoma;

- the presence of ocular trauma or other abnormalities, such as microcornea, microphthalmia, persistent hyperplastic primary vitreous, Peters anomaly, congenital aniridia, Marfan syndrome, lens dislocation, retinitis pigmentosa, high myopia, fundus lesions, rubella, and Lowe syndrome.

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 the incidence of suspected glaucoma/glaucoma after congenital cataracts A Kaplan-Meier analysis was used. 3 years
Primary Risk Factors of suspected glaucoma/glaucoma after congenital cataracts Cox regression analysis was assessed 3 years
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