Study on Effective Mydriasis in Premature Infants

Sponsor

Georgetown University (Other)

Overall Status

Completed

CT.gov ID

NCT01054027

Collaborator

(none)

Enrollment

Location

Arms

Duration (Months)

1.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to compare the dilating effect of 0, 1, 2 or 3 drops of mydriatic (pupil dilating) in premature infants undergoing routine retinal (eye) screening exams for Retinopathy of Prematurity (ROP).

Condition or Disease	Intervention/Treatment	Phase
Retinopathy of Prematurity (ROP)	Drug: 1% phenylephrine and 0.2% cyclopentolate	N/A

Detailed Description

Premature infants need to have eye exams starting at about 4 weeks of age and continuing until their retinas (membrane at the back of the eye which collects and transfers light) is fully grown. These exams are done to see if they have developed ROP, a disease which can lead to blindness if not treated.

The ophthalmologist (eye doctor) looks through the enlarged pupil (opening at the front of the eye) to see the retina. The drug that is used to dilate the pupil, Cyclomydril, has been shown to have side effects in premature infants. No literature has shown what the optimal dose is for premature babies. Nursery policy is to give 3 drops of Cyclomydril in each eye, at 5 minute intervals, 45-60 minutes before a scheduled eye exam. We sought to reduce the dose without delaying the exam for an under-sized pupil.

In the study, each infant is randomized at the time of the exam to receive either 0, 1 or 2 drops of Cyclomydril in the left eye and 3 drops in the right eye to serve as their own control. The zero-drop group was created to test the contralateral (opposite eye) effect of 3 drops in the right eye. Pupil dilation size is measured using the Colvard pupillometer by a Pediatric Ophthalmologist examiner (G.V.V.) who was not masked to study group assignment.

Measures of pupil size are done at baseline (before any drops given), 45, 90 and 120 minutes after the first drop was given. ROP screening exam is done at the first opportunity to visualize the posterior and peripheral retina.

Additional drops are given at 120 minutes if the observer is unable to complete the exam prior to that point.

Study Design

Study Type:

Interventional

Actual Enrollment :

15 participants

Allocation:

Randomized

Intervention Model:

Factorial Assignment

Masking:

None (Open Label)

Primary Purpose:

Screening

Official Title:

A Randomized Controlled Trial to Determine the Lowest Effective Dose for Adequate Mydriasis in Premature Infants

Study Start Date :

Mar 1, 2007

Actual Primary Completion Date :

Nov 1, 2007

Actual Study Completion Date :

Mar 1, 2008

Arms and Interventions

Arm	Intervention/Treatment
Experimental: 0 Drop Left eye dose	Drug: 1% phenylephrine and 0.2% cyclopentolate given as drops, prior to eye exam Other Names: Cyclomydril
Experimental: 1 Drop Left eye dose	Drug: 1% phenylephrine and 0.2% cyclopentolate given as drops, prior to eye exam Other Names: Cyclomydril
Experimental: 2 drop Left eye dose	Drug: 1% phenylephrine and 0.2% cyclopentolate given as drops, prior to eye exam Other Names: Cyclomydril
Active Comparator: 3 drops Right eye dose for all groups	Drug: 1% phenylephrine and 0.2% cyclopentolate given as drops, prior to eye exam Other Names: Cyclomydril