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Clinical trialNCT00212134CompletedInterventional

Infant Aphakia Treatment Study (IATS)

SponsorStanford UniversityEnrollment114Congenital Cataract
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The primary purpose is to determine whether infants with a unilateral congenital cataract are more likely to develop better vision following cataract extraction surgery if they undergo primary implantation of an intraocular lens or if they are treated primarily with a contact lens. In addition, the study will compare the occurrence of postoperative complications and the degree of parental stress between the two treatments.
clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

13 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Stanford University

    Palo Alto, California, United States

  • Miami Children'S Hospital

    Miami, Florida, United States

  • Emory Eye Center

    Atlanta, Georgia, United States

  • Indiana University Medical Center

    Indianapolis, Indiana, United States

  • Harvard University

    Boston, Massachusetts, United States

  • University of Minnesota

    Minneapolis, Minnesota, United States

  • Duke University Eye Center

    Durham, North Carolina, United States

  • Cleveland Clinic Foundation

    Cleveland, Ohio, United States

  • Oregon Health and Science University

    Portland, Oregon, United States

  • Medical University of South Carolina

    Charleston, South Carolina, United States

  • Vanderbilt University

    Nashville, Tennessee, United States

  • Pediatric Ophthalmology, P.A.

    Dallas, Texas, United States

  • Baylor University

    Houston, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Dec 2004
Primary completion
31 Aug 2020
Completion
31 Aug 2020
Last update posted
24 Jul 2024
Registered enrollment
114
Registry id
NCT00212134
clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.