Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00212134 · ClinicalTrials.gov registry record · NA

Infant Aphakia Treatment Study (IATS)

A NA study, sponsored by Stanford University.

Completed
Registry status
NA
Development phase
114
Enrollment target

NCT00212134: Completed NA study, sponsored by Stanford University.

NCT00212134 is a NA study that has completed, run by Stanford University. The registered enrollment target is 114 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT00212134, a NA study, has completed, sponsored by Stanford University.

COMPLETED
Registry status
NA
Development phase
114 participants
Enrollment target

Study Summary

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.

Primary Outcome

Visual acuity was measured by standard objective testing procedures at 12 months of age. Monocular grating acuity was assessed by the traveling examiner with the Teller Acuity Cards. This test uses cards with black-on-white lines of varying widths and a set distance apart in a square with fixed dimensions, so the thinner the lines, the more there will be on any given card (cycles/cm). The ability to see thinner lines indicates better vision. The cards with lines are presented simultaneously with

Interventions

  • DEVICE Contact lens correction of aphakia
  • DEVICE Intraocular lens implantation

Trial Details

FieldValue
Enrollment Target 114 participants
Start Date 2004-12
Est. Completion 2020-08-31
Phase NA
Stanford University

1,744 total trials

What the finished NCT00212134 record still lists

NCT00212134 is an interventional study that assigns participants to a tested intervention. The registered 114 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 2 interventions - of which Contact lens correction of aphakia is the first listed.

NCT00212134 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00212134 about?

NCT00212134 is a clinical study titled "Infant Aphakia Treatment Study (IATS)". 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 ...

What is the current status of trial NCT00212134?

This trial is currently completed. It is a NA study. The enrollment target is 114 participants. The study started on 2004-12. Estimated completion is 2020-08-31.

What interventions are being tested in trial NCT00212134?

The interventions under investigation include: Contact lens correction of aphakia (DEVICE), Intraocular lens implantation (DEVICE).

Who is sponsoring clinical trial NCT00212134?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00212134's enrollment target sits among peer trials

114 811th of 2000 higher than 1,188 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04522791 · 114 participants · Phase 2

    Breathing, Relaxation, Attention Training, & Health in Older Adults (BREATHE)

  • NCT04875052 · 114 participants · NA

    Vibration and Post-traumatic Osteoarthritis Risk Following ACL Injury

  • NCT05100342 · 114 participants

    Prospective Validation of a Points Score System Predicting 30-day Survival

  • NCT05224089 · 114 participants · Phase 4

    Bilateral TAP and RS Blocks Using Liposomal Bupivacaine/Bupivacaine vs. Regular Bupivacaine in Laparoscopic Colectomy

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00212134, the US trial registry maintained by the National Library of Medicine. NCT00212134 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.