A Scan Ultrasonography in the Evaluation of Retinopathy of Prematurity

Retinopathy of Prematurity Clinical Trial

Official title:

A Scan Ultrasonography in the Evaluation of Retinopathy of Prematurity

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01335113
• Other study ID #: 19891
• Status: Terminated
• Start date: October 2010
• Est. completion date: October 1, 2015

Study information

• Verified date: July 2020
• Source: Stanford University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of the investigators study is to determine the relationship between the length of the eye and the rate of change in eye length at each visit with progression of retinopathy of prematurity.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 1
• Est. completion date: October 1, 2015
• Est. primary completion date: October 1, 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• neonates being screened for retinopathy of prematurity

Exclusion Criteria:

• medically unstable neonates

Related Conditions & MeSH terms

• Premature Birth
• Retinal Diseases
• Retinopathy of Prematurity

Locations

Country	Name	City	State
United States	University of Miami	Miami	Florida

Sponsors (2)

Lead Sponsor	Collaborator
Stanford University	University of Miami

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	axial length	axial length as measured by a scan ulstrasonography	one year
Secondary	anterior corneal curvature	anterior corneal curvature as measured by keratometer	one year
Secondary	wide angle fundus photography	wide angle fundus photography by RetCam camera	one year