The study will measure the effects of eye exams on markers of stress in the urine. In
addition, measurements will be taken to show the effects of stress on brain activity, O2
sats, and blood flow.
We will connect you to the doctor responsible for this trial and help you get more information.
Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT02415205
Ages eligible for Study
24 Weeks to 32 Weeks
Genders eligible for Study
Accepts Healthy Volunteers
Premature infants between 24 -32 weeks of gestational age
Infants scheduled for laser eye surgery on the day of the examination
Infants with intraventricular hemorrhage ≥ grade 3 (Papile classification) diagnosed by head ultrasound
Infants receiving the following medications: morphine, fentanyl, methadone, midazolam, lorazepam, muscle relaxants, phenobarbital, phenytoin, levetiracetam
Renal injury defined with plasma creatinine > 1.5 mg/dL
Severe cyanotic congenital heart disease
Unstable respiratory distress (hypoxemia PaO2 < 50 mm Hg or SpO2 < 90%)
All locations for NCT02415205
United States (1)
Loma Linda University Children's Hospital
Loma Linda, California, United States, 92354
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View full eligibility
Tris trial is registered with FDA with number: NCT02415205. The sponsor of the trial is Loma Linda University and it is looking for 80 volunteers for the current phase.
Official trial title: Pain and Stress Assessment and ROP Screening Examination in Premature Infants
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