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Completed No phase listed Observational

An Ocular Safety Study of Ivacaftor-Treated Pediatric Patients 11 Years of Age or Younger With Cystic Fibrosis

ClinicalTrials.gov ID: NCT01863238

Public ClinicalTrials.gov record NCT01863238. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 4:12 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is designed to evaluate the risk of cataracts (lens opacities) and describe the best corrected distance vision (with glasses/contacts for those who wear them) of pediatric patients with Cystic Fibrosis who are 11 years of age or younger at the time of ivacaftor treatment initiation and are receiving or planning to receive commercially-available ivacaftor in the US.

Study identification

NCT ID
NCT01863238
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
95 participants

Conditions and interventions

Interventions

Other · Drug

Eligibility (public fields only)

Age range
6 Years to 11 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2013
Primary completion
Apr 30, 2016
Completion
Apr 30, 2016
Last update posted
Aug 22, 2016

2013 – 2016

United States locations

U.S. sites
38
U.S. states
30
U.S. cities
38
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Tucson Arizona
Not listed Long Beach California
Not listed Aurora Colorado
Not listed Wilmington Delaware
Not listed St. Petersburg Florida
Not listed Boise Idaho
Not listed Chicago Illinois
Not listed Indianapolis Indiana
Not listed Kansas City Kansas
Not listed Louisville Kentucky
Not listed Portland Maine
Not listed Boston Massachusetts
Not listed Ann Arbor Michigan
Not listed Detroit Michigan
Not listed Minneapolis Minnesota
Not listed Columbia Missouri
Not listed Kansas City Missouri
Not listed Omaha Nebraska
Not listed Rochester New York
Not listed Akron Ohio
Not listed Cincinnati Ohio
Not listed Toledo Ohio
Not listed Oklahoma City Oklahoma
Not listed Portland Oregon
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Providence Rhode Island
Not listed Charleston South Carolina
Not listed Knoxville Tennessee
Not listed Nashville Tennessee
Not listed Fort Worth Texas
Not listed Houston Texas
Not listed Salt Lake City Utah
Not listed Charlottesville Virginia
Not listed Seattle Washington
Not listed Spokane Washington
Not listed Morgantown West Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01863238, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 22, 2016 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01863238 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →