Clinical Observation of the Transscleral Suture Fixation of Posterior Chamber Intraocular Lens in Eyes With Inadequate Capsule Support

Second Affiliated Hospital, School of Medicine, Zhejiang University21 enrolled

Overview

To present the follow-up outcomes of transscleral suture fixation of posterior chamber intraocular lens (PCIOL) in eyes with inadequate capsule support.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Absence of Capsule Support Aphakia

Interventions

posterior chamber intraocular lens implantationPROCEDURE

patients who underwent transscleral sutured posterior chamber intraocular lens implantation

Eligibility

Sex: ALLMin age: 10 YearsMax age: 80 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Patients who underwent transscleral suture fixation of PCIOL 2. Time between the primary surgeries was at least 3 months Exclusion Criteria: 1. Active intraocular inflammation 2. The intraocular pressure (IOP) was higher than 25 mmHg 3. The endothelial cell count (ECC) was more than 1,200 cells/mm2

Locations (1)

Second Affiliated Hospital, Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

Outcomes

Primary Outcomes

Visual function

Best corrected visual acuity (BCVA) measured using a decimal chart

Time frame: 1day postoperation

Visual function

Best corrected visual acuity (BCVA) measured using a decimal chart

Time frame: 1 week postoperation

Visual function

Best corrected visual acuity (BCVA) measured using a decimal chart

Time frame: 1 month postoperation

Visual function

Best corrected visual acuity (BCVA) measured using a decimal chart

Time frame: 3 month postoperation

Visual function

uncorrected distance visual acuity (UDVA) measured using a decimal chart

Time frame: 1 day postoperation

Visual function

uncorrected distance visual acuity (UDVA) measured using a decimal chart

Time frame: 1 week postoperation

Visual function

uncorrected distance visual acuity (UDVA) measured using a decimal chart

Time frame: 1 month postoperation

Visual function

uncorrected distance visual acuity (UDVA) measured using a decimal chart

Time frame: 3 month postoperation

Secondary Outcomes

intraocular pressure

Data from ClinicalTrials.gov

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