Comparing two methods for calculating intraocular lens power during cataract surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This intervention compares the accuracy of intraoperative aberrometry (ORA) against the Barrett Universal II preoperative calculation for determining intraocular lens power in patients undergoing cataract surgery. The study will involve randomization and blinding of participants to ensure unbiased results. Researchers will assess changes in spherical equivalent and uncorrected distance visual acuity at 90 days post-surgery to evaluate the effectiveness of each method.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* patients with senile cataract, patients undergoing phacoemulsification, complete biometric profile, axial length calculated by interferometer.

Exclusion Criteria:

* glaucoma, uncontrolled diabetic retinopathy, pseudoexfoliation syndrome, aged macular degeneration , dry eye syndrome, other ocular pathologies.

Where it's running

• Instituto de oftalmología Fundación Conde de Valenciana
  Mexico City, Cuauhtemoc, Mexico Recruiting

Study contacts

• Principal investigator: Angel Nava - Castañeda, Md — Instituto de Oftalmologia Conde de Valenciana
• Study coordinator: Diego Zamora - de la Cruz, Md
• Email: DIEGO.ZAMORA@INSTITUTODEOFTALMOLOGIA.ORG
• Phone: 5554421700

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.