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Clinical Trial Summary

Aim: The aim of the study is to determine the effect of non-nutritive sucking on pain during examination for retinopathy of prematurity. Method: The study is conducted as a randomized controlled trial. The population of the study is premature newborn who treatment in a neonatal intensive unit. The premature newborns divided into two groups as an intervention and control group according to randomization. After the randomization, non-nutritive sucking is applied to the intervention group. No method is applied to the control group.


Clinical Trial Description

A topical anesthetic will be applied to all premature newborns 30 seconds before eye examination. Non-nutritive sucking is applied to the intervention group during the examination for retinopathy of prematurity. No method is applied to the control group during the examination for retinopathy of prematurity ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04463927
Study type Interventional
Source Adiyaman University Research Hospital
Contact
Status Completed
Phase N/A
Start date May 10, 2020
Completion date October 9, 2020

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