COMPLETED

iCare IC1000 Alignment Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The primary objective of this study is to evaluate the performance of the alignment feature of iCare IC1000 tonometer.

Official Title

iCare IC1000 Alignment Study

Quick Facts

Study Start:2025-05-22
Study Completion:2025-08-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT07022054

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age ≥ 18 years
  1. 1. Subjects with only one functional eye
  2. 2. Central corneal scarring
  3. 3. Microphthalmos
  4. 4. Buphthalmos
  5. 5. Contact lens use during measurement or hard lenses 24h prior to measurement
  6. 6. Dry eyes (clinically significant)
  7. 7. Nystagmus
  8. 8. Keratoconus
  9. 9. Any other corneal or conjunctival pathology or infection relevant to this study
  10. 10. Coloboma or other pupil deformation

Contacts and Locations

Study Locations (Sites)

Clear Vue Laser Eye Center
Lake Worth, Florida, 33467
United States

Collaborators and Investigators

Sponsor: Icare Finland Oy

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-22
Study Completion Date2025-08-05

Study Record Updates

Study Start Date2025-05-22
Study Completion Date2025-08-05

Terms related to this study

Additional Relevant MeSH Terms

  • Intraocular Pressure