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Effect of the Timing of Cataract Surgery on Complications in Patients With Bilateral Congenital Cataracts

Effect of the Timing of Lens-removal Cataract Surgery on Postoperative Complications Rate Among Patients With Bilateral Congenital Cataracts

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02581046
Enrollment
61
Registered
2015-10-20
Start date
2011-01-31
Completion date
2013-12-31
Last updated
2015-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract

Brief summary

Congenital cataract is an important treatable cause of visual handicap in childhood throughout the world. Successful management of childhood cataract is dependent on individualized treatment strategies and rigorous postoperative supervision for adverse complication. In this trial, we aimed to compare the difference of postoperative outcome between surgical timing at age of 3 month and 6 month. Patients enrolled into the study will be followed for two year and will have study visits at 1 day, 1 week, 1 month, 3 month, 6 month, 9 month, 12 month, 18month and 24month postoperatively.

Detailed description

Congenital cataract is a priority of Vision 2020: the Right to Sight, the global initiative to reduce the world's burden of avoidable blindness, because it is an important treatable cause of visual handicap in childhood throughout the world. Successful management of childhood cataract is dependent on individualized treatment strategies and postoperative supervision for adverse complication is also essential. The timing of surgery of childhood cataract depends on the etiology and on the degree of visual interference. Severe bilateral cataracts with significant obstruction of the visual axis must be treated and surgery is recommended as soon as possible after discovery. Several previous studies claimed that ideally cataracts should be removed before 3 months of age, while the result of recent researches shows that too early intervention for cataract surgery seems aggressive and would cause serious complications, which might cause poor long-term visual outcomes. Therefore, in order to control childhood blindness and severe visual impairment in China, it is of great importance to ensure that pediatric patients with cataract could have good timing of surgery, postoperative rigorous supervision, accurate optical rehabilitation and comprehensive treatment of amblyopia. In this trial, we aimed to compare the difference of postoperative outcome between surgical timing at age of 3 month and 6 month. Patients enrolled into the study will be followed for two year and will have study visits at 1 day, 1 week, 1 month, 3 months, 6 months, 9 months, 12 months, 18months and 24months after cataract surgery.

Interventions

PROCEDUREPhacomulsification lens removal cataract surgery without Intraocular lens(IOL) implantation at the age of 3month of the patients

The surgical timing of phacoemulsification is perform at the age of 3 month of the patients. During Phacoemulsification, viscoelastic materials and anterior lens capsule are used to protect corneal endothelial cells.

PROCEDUREPhacomulsification lens removal cataract surgery without Intraocular lens(IOL) implantation at the age of 6 month of the patients

The surgical timing of phacoemulsification is perform at the age of 6 month of the patients. During Phacoemulsification, viscoelastic materials and anterior lens capsule are used to protect corneal endothelial cells.

All patients received subconjunctival dexamethasone (2 mg) during surgery, and all surgeries were performed under general anesthesia.

Sponsors

Ministry of Health, China
CollaboratorOTHER_GOV
Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
No minimum to 3 Months
Healthy volunteers
No

Inclusion criteria

* Children diagnosis with bilateral congenital cataract for entire lens without other ocular abnormality * No more than 3 month old * Have signed a consent form * Can be followed

Exclusion criteria

* Children not identified with congenital cataract * Have not signed consent form * Be not able to be followed

Design outcomes

Primary

MeasureTime frame
Change from baseline in the central subfield thickness (CST) measured by Optical Coherence Tomography(OCT)during surgery,postoperation time:1day,1week,1month,3month,6month,9month,12month,18month,24month
Change from baseline in the thickness of the inner retinal layer regions measured by Optical Coherence Tomography(OCT)during surgery,postoperation time:1day,1week,1month,3month,6month,9month,12month,18month,24month
Change from baseline in the thickness of the outer retinal layer regions measured by Optical Coherence Tomography(OCT)during surgery,postoperation time:1day,1week,1month,3month,6month,9month,12month,18month,24month

Secondary

MeasureTime frame
Number of participants with abnormal intraocular pressure or diagnosis with secondary glaucoma2 year after surgery
Number of participants undergoing Nd:YAG laser capsulotomy due to severe posterior capsular opacification(PCO)2 year after surgery

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026