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Predicted Astigmatism Prediction in Limbal Relaxing Incisions for Astigmatism Correction during Cataract Surgery

Predicted Refractive Astigmatism in Limbal Relaxing Incisions for Astigmatism Correction during Cataract Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114105
Enrollment
Unknown
Registered
2025-12-08
Start date
2025-12-08
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Cataract

Interventions

The experimental group:Routine cataract surgery combined with limbal relaxing incisions using predicted postoperative astigmatism as the reference for astigmatism correction
The control group:Routine cataract surgery combined with limbal relaxing incisions using simulated keratometry as the reference for astigmatism correction.

Sponsors

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age over 18 years. 2. Regular corneal astigmatism, with predicted postoperative astigmatism or simulated keratometry greater than 0.5 D. 3. Participants must be in relatively good general health to ensure the safety and feasibility of the surgical procedure. 4. Participants must be willing to undergo preoperative assessments and comply with postoperative follow-up observations.

Exclusion criteria

Exclusion criteria: 1. Presence of irregular corneal astigmatism due to corneal diseases (e.g., keratoconus, corneal degeneration, corneal scar) or a history of corneal surgery (e.g., corneal refractive surgery, corneal transplantation). 2. History of severe ocular diseases, such as lens subluxation/dislocation, endophthalmitis, or glaucoma. 3. History of other ocular surgeries, such as intraocular surgery, or a history of ocular trauma. 4. Patients intolerant to the surgical procedure. 5. Patients who experience intraoperative or postoperative complications.

Design outcomes

Primary

MeasureTime frame
Postoperative uncorrected visual acuity;Postoperative best corrected visual acuity;Postoperative astigmatism value;

Secondary

MeasureTime frame
Refraction spherical equivalent;Keratometry;

Countries

China

Contacts

Public ContactQu Chao

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital

lucyqujefferson@qq.com+86 28 8739 3700

Outcome results

None listed

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