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NCT07475832 · ClinicalTrials.gov registry record

Comparison of Two Biometers in Dense Cataracts

A clinical trial, sponsored by Berkeley Eye Center.

Completed
Registry status
61
Enrollment target

NCT07475832 is a clinical trial that has completed, run by Berkeley Eye Center. The registered enrollment target is 61 participants.

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The verdict

NCT07475832 has completed, sponsored by Berkeley Eye Center.

COMPLETED
Registry status
61 participants
Enrollment target

Study Summary

This single-center, ambispective, observational study evaluates axial length acquisition in eyes with dense cataracts using the ARGOS swept-source optical coherence tomography biometer compared with the IOLMaster 700. Eligible subjects are pseudophakic adults who previously underwent complex cataract surgery because of poor visualization or poor red reflex from dense lens opacity and who had pre-operative biometry performed with both devices, with or without manual immersion A-scan ultrasonography. Enrolled subjects return for postoperative repeat biometry to confirm pre-operative measurements and to assess whether availability of an ARGOS axial length measurement may reduce the need for manual ultrasound A-scans in similar dense cataract cases. The planned sample size justification estimated that 61 patients were needed for statistical power, while 68 were originally targeted to allow for attrition in the prospective portion.

Interventions

  • DIAGNOSTIC_TEST IOLMaster 700
  • DIAGNOSTIC_TEST ARGOS biometer

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2023-10-11
Est. Completion 2025-10-15

Sponsor

Berkeley Eye Center

8 total trials

What the Registry Record Tells You About NCT07475832

The ClinicalTrials.gov registry entry for NCT07475832 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 61 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Berkeley Eye Center, which has 8 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which IOLMaster 700 is the first listed.

NCT07475832 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07475832 about?

NCT07475832 is a clinical study titled "Comparison of Two Biometers in Dense Cataracts". This single-center, ambispective, observational study evaluates axial length acquisition in eyes with dense cataracts using the ARGOS swept-source optical coherence tomography biometer compared with the IOLMaster 700. Eligible subjects are pseudophakic adults who previously underwent complex catarac...

What is the current status of trial NCT07475832?

This trial is currently completed. The enrollment target is 61 participants. The study started on 2023-10-11. Estimated completion is 2025-10-15.

What interventions are being tested in trial NCT07475832?

The interventions under investigation include: IOLMaster 700 (DIAGNOSTIC_TEST), ARGOS biometer (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT07475832?

This trial is sponsored by Berkeley Eye Center, which has 8 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.