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Effect of Different Needle Insertion Positions on the Clinical Efficacy of YAMANE technique of Intraocular Lens: A Randomized Controlled Trial

Effect of Different Needle Insertion Positions on the Clinical Efficacy of YAMANE technique of Intraocular Lens: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111353
Enrollment
Unknown
Registered
2025-10-30
Start date
2025-10-30
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

congenital ectopia lentis

Interventions

Intervention group:YAMANE Technique (Suture Needle Insertion at 2.5 mm Posterior to the Limbus)
Control group:YAMANE Technique (Suture Needle Insertion at 2 mm Posterior to the Limbus)

Sponsors

The Zhongshan Ophthalmic Center,Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 4-18 years (regardless of gender) who meet the indications for YAMANE-style scleral interlaminar fixation of intraocular lens (IOL); 2.Patients who can complete a follow-up period of at least 3 months after surgery; 3.Patients or their legal guardians who provide informed consent to participate in this study;

Exclusion criteria

Exclusion criteria: 1.Patients with concurrent secondary glaucoma, retinal detachment, strabismus, or other relevant ocular complications (excluding refractive errors); 2.Patients participating in other trials that may affect the results of this study;

Design outcomes

Primary

MeasureTime frame
Refractive Predictive Error of Patients at the 3-month Postoperative Follow-up;

Secondary

MeasureTime frame
Incidence of Postoperative Complications at the 3-Month Postoperative Follow-up;Corneal Endothelial Cell Count of Patients at the 3-Month Postoperative Follow-up;IOL Tilt and Decentration in Patients at the 3-Month Postoperative Follow-up;Uncorrected Visual Acuity (UCVA) and Best-Corrected Visual Acuity (BCVA) of Patients at the 3-Month Postoperative Follow-up;

Countries

China

Contacts

Public ContactGuangming Jin

The Zhongshan Ophthalmic Center,Sun Yat-sen University

jingm@mail2.sysu.edu.cn+86 20 66604125

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026