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A clinical study: The timing of Laser iridectomy impact on ICL postoperative visual quality and the safety .

A clinical study: The timing of Laser Iridectomy impact on ICL postoperative visual quality and the safety .

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004743
Enrollment
Unknown
Registered
2014-06-04
Start date
2014-06-09
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

high myopia

Interventions

Experimental group:Laser iridectomy 2h before ICL surgery
Control group:Laser iridectomy 1 week before ICL surgery

Sponsors

Department of Ophthalmology, Research Institute of Field Surgery, Da Ping Hospital, Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Aged>18 years, and diopter number stable for more than one year; (2) Glaucoma, diabetes or autoimmune diseases; (3) Anterior chamber distanceACD>3mm; (4) Corneal endothelial count >2500/ram; (5) IOP: 1020 mmHg (1mmHg=0.133kPa).

Exclusion criteria

Exclusion criteria: Intraocular surgery, corneal disease, glaucoma, uveitis, diabetic retinopathy and other eye diseases.

Design outcomes

Primary

MeasureTime frame
IOP;Corneal endothelial count;BCVA;Surgical complication;—

Countries

China

Contacts

Public ContactJian Ye

Department of Ophthalmology, Research Institute of Field Surgery, Da Ping Hospital, Third Military Medical University

yejian1979@163.com+86 023 68757766

Outcome results

None listed

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