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Full-Range Visual Acuity After Functional Intraocular Lens Implantation in Patients with Low to Moderate Myopia and Cataract: A Clinical Study

Full-Range Visual Acuity After Functional Intraocular Lens Implantation in Patients with Low to Moderate Myopia and Cataract: A Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126973
Enrollment
Unknown
Registered
2026-06-22
Start date
2026-06-25
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Cataract

Interventions

Control group:None
Multifocal intraocular lens or combined EDoF intraocular lens implantation group:None
Monofocal intraocular lens implantation group:None
Observation group:None

Sponsors

Tianjin Medical University Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Multifocal intraocular lens or combined EDoF implantation group Multifocal intraocular lens or combined EDoF implantation group for patients with moderate to low myopia undergoing cataract surgery at our hospital. (1) Sign a written informed consent form; (2) Preoperative equivalent spherical mirror (SE) is -0.50D~-6.00D, astigmatism < = 1.0 D; (3) Prefer to remove the lens completely after surgery; (4) Implantation of multifocal intraocular lens or multifocal intraocular lens combined with EDoF type intraocular lens; (5) No history of other eye diseases. 2. Monofocal intraocular lens implantation group Moderate to low-degree myopia patients undergoing cataract surgery at our hospital (1) Sign a written informed consent form; (2) Preoperative equivalent spherical mirror (SE) was -0.50D~-6.00D, astigmatism <=1.0D; (3) Those who wish to maintain the habit of seeing far and wearing nearsighted glasses; (4) Implantation of a single-lens intraocular lens; (5) No history of other eye diseases. 3. Monofocal enhanced intraocular lens implantation group Moderate to low-degree myopia patients undergoing cataract surgery at our hospital. (1) Sign a written informed consent form; (2) Preoperative equivalent spherical mirror (SE) is -0.50D~-6.00D, astigmatism <= 1.0 D; (3) Irregular wearing of myopia glasses for years before surgery, hoping for postoperative work distance and indoor lens removal; (4) Postoperative target equivalent spherical mirror is -1.50D~-2.00D; (5) Implantation of a monofocal enhanced intraocular lens; (6) No history of other eye diseases. 4. Control Group: Moderate to low-degree myopia patients undergoing cataract surgery at our hospital. (1) Sign a written informed consent form; (2) Preoperative equivalent spheroflexia (SE) was -0.50D~-6.00D, astigmatism <= 1.0D; (3) Irregular wearing of myopia glasses for years before surgery, hoping for postoperative work distance and indoor lens removal; (4) Postoperative target equivalent spherical mirror is -1.50D~-2.00D; (5) Implantation of a conventional single-lens intraocular lens; (6) No history of other eye diseases.

Exclusion criteria

Exclusion criteria: 1. Multifocal or combined EDoF intraocular lens implantation group (1) Has macular disease, diabetic retinopathy, or other fundus diseases; (2) Has glaucoma, corneal disease, scleral disease, etc.; (3) Has neurological diseases that affect visual quality; (4) Has a history of other eye surgeries; (5) Cannot cooperate with relevant examinations. 2. Monofocal intraocular lens implantation group (1) Has macular disease, diabetic retinopathy, or other fundus diseases; (2) Has glaucoma, corneal disease, scleral disease, etc.; (3) Has neurological diseases that affect visual quality; (4) Has a history of other eye surgeries; (5) Cannot cooperate with relevant examinations. 3. Enhanced monofocal intraocular lens implantation group (1) Has macular disease, diabetic retinopathy, or other fundus diseases; (2) Has glaucoma, corneal disease, scleral disease, etc.; (3) Has neurological diseases that affect visual quality; (4) Has a history of other eye surgeries; (5) Cannot cooperate with relevant examinations

Design outcomes

Primary

MeasureTime frame
Uncorrected near vision at a long distance (33cm);Uncorrected intermediate vision from a long distance (60cm);Uncorrected distance vision (6m);Subjective visual quality;

Secondary

MeasureTime frame
Defocus curve;Objective visual quality;

Countries

China

Contacts

Public ContactFang Tian

Tianjin Medical University Eye Hospital

tianfang1216@126.com+86 22 86428703

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026