Clinical Trials Logo

Retinopathy of Prematurity clinical trials

View clinical trials related to Retinopathy of Prematurity.

Filter by:

NCT ID: NCT03448640 Completed - Clinical trials for Retinopathy of Prematurity

Efficacy of Mydriatic Drops in Premature Infants

Start date: January 15, 2016
Phase: N/A
Study type: Observational

Because of the neonatologists reported that some infants had suffered from vomiting, bradycardia, hypotonia, and aspiration risk about 30-60 minutes after the fundus examination in the intensive care unit. The investigators observed the pupil dilation effects and side effects of tipple instillation of phenylephrine 2.5% plus tropicamide 0.5% ophthalmic drop combination which the investigators routinely used in ROP examination.

NCT ID: NCT03399825 Withdrawn - Clinical trials for Diabetic Retinopathy

Optical Coherence Tomography Angiography (OCT-A) in Children (≥ 6 <14 Years of Age)

OCTAC
Start date: January 2018
Phase:
Study type: Observational

Comparison of OCTA to conventional imaging modalities for the diagnosis of eye diseases in children

NCT ID: NCT03347799 Completed - Clinical trials for Retinopathy of Prematurity

WINROP Algorithm Validation for Retinopathy Screening in a Cohort of Premature Infants

WINROP
Start date: July 1, 2012
Phase:
Study type: Observational

When a child was born too early, it is more likely to develop an alteration of its visual function than in the case of term birth. Significant visual disturbances are found in 3% of children born prematurely, but visual impairment can be very severe, up to the loss of vision in case of retinopathy of prematurity (ROP) in the most immature infants. The introduction of screening surveillance systems, such as WINROP software, might reduce the need for stressful eye examination in low risk neonates. This retrospective study aimed at validating the WINROP algorithm in a cohort of premature infants, born below 32 weeks of gestation, who had systematic eye examination for ROP screening over 4 year period.

NCT ID: NCT03334513 Completed - Clinical trials for Retinopathy of Prematurity

Refractive Error and Biometry in Retinopathy of Prematurity

Start date: April 1, 2011
Phase: N/A
Study type: Observational

The investigators compared long-term refractive and biometric outcomes in children with retinopathy of prematurity who received two different anti-vascular endothelial growth factor agents.

NCT ID: NCT03274596 Completed - Clinical trials for Retinopathy of Prematurity

Effect of Vitamin E for Prevention of Retinopathy of Prematurity: A Randomized Clinical Trial.

Start date: March 1, 2013
Phase: N/A
Study type: Interventional

The retinopathy of prematurity (ROP) is a public health problem, the main causes of ROP are prematurity, use of oxygen, malnutrition and oxidative stress. Vitamin E was used beforehand however its use was stopped because of its association with sepsis and enterocolitis caused by the excipient of vitamin E. The purpose of this study is to use vitamin E to prevent ROP, without the previously used excipients.

NCT ID: NCT03253263 Recruiting - Clinical trials for Bronchopulmonary Dysplasia

A Clinical Efficacy and Safety Study of OHB-607 in Preventing Bronchopulmonary Dysplasia in Extremely Premature Infants

Start date: May 9, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if an investigational drug can prevent Bronchopulmonary Dysplasia, reducing the burden of chronic lung disease in extremely premature infants, as compared to extremely premature infants receiving standard neonatal care alone.

NCT ID: NCT03201588 Completed - Clinical trials for Ophthalmological Disorder

Multi-Center Study to Determine the Role of Fatty Acids in Serum in Preventing Retinopathy of Prematurity (MDM)

MDM
Start date: December 15, 2016
Phase: N/A
Study type: Interventional

The study is a Randomized Intervention, Multi-Center Study to Determine the Role of Fatty Acids in Serum and Breast Milk in preventing Retinopathy of Prematurity Subjects who meet all inclusion and none of the exclusion criteria will be enrolled into the study. Upon entry into the study, subjects will be randomized and given a unique subject number. A randomized intervention study of 105+105 (number based on power analysis regarding up to date ROP frequency, see 5.1 and 11.1) infants without major malformations born with a gestational age less than 28 weeks + 0 days will be performed.

NCT ID: NCT03154723 Completed - Clinical trials for Retinopathy of Prematurity

Effects of Early Vitamin A Supplementation on the Risk for Retinopathy of Prematurity in Extremely Preterm Infants

Start date: August 1, 2015
Phase: N/A
Study type: Interventional

Retinopathy of prematurity (ROP) is a common retinal neovascular disorder and major cause of vision impairment or blindness, despite current treatment of late stage ROP. Because the visual disorders after treatment are often poor, preventive therapy for ROP is still lacking. Although ROP is a multifactorial disease, the altered regulation of vascular endothelial growth factor (VEGF) and insulin-like growth factor (IGF-1) have been implicated in the pathogenesis of ROP. Vitamin A is one of the most important micronutrients affecting the health of children. Supplementing newborn infants with vitamin A within the first 2 days of life reduced infant mortality by almost 25%, with the greatest benefit to those of low birth weight. Vitamin A has been used in this population prophylactically for chronic lung disease with the large doses and no reported significant adverse effect exists. It is suggested that vitamin A-retinoids and their active metabolite, retinoic acid (RA) have highly potent antiangiogenic activity by inhibiting VEGF expression. Vitamin A (retinol) is converted into retinoic acid in cells. However, the significance of Vitamin A administration has not been investigated to our knowledge in an experimental ROP infant. The aim of this study was to perform prospective, multicenter, randomized design to demonstrate the preventive effect of Vitamin A on ROP.

NCT ID: NCT03148132 Completed - Premature Birth Clinical Trials

VEGF Concentrations After Intravitreal Bevacizumab vs Ranibizumab as a Treatment for Type 1 ROP

Start date: May 23, 2017
Phase: Phase 4
Study type: Interventional

The Retinopathy of Prematurity (ROP) is one of the leading causes of blindness on the pediatric age worldwide. This pathology is characterized for arrest of the normal vascular and neuronal retina that because of pathological compensatory mechanisms results in proliferation of vascular tissue that grow in the limit between the vascular retina and the avascular retina. The ET-ROP group classified the ROP by those who need treatment immediately or those who doesn't need treatment, The classification is the following Type 1 ROP-->ROP zone I any stage with plus, zone I stage 3 without plus, zone II stage 2 y 3 with plus Type 2 ROP --> Zone 1, Stage 2 or 3 without plus, and Zone II, stage 3 without plus. The treatment is begun on patient with type 1 ROP and type 2 ROP is maintained in observation.

NCT ID: NCT03115255 Completed - Clinical trials for Infant, Premature, Diseases

Serum Vascular Endothelial Growth Factor in Infants With Intravitreal Ranibizumab

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

To determine the serum concentrations of ranibizumab and vascular endothelial growth factor (VEGF) in infants with retinopathy of prematurity (ROP) who received intravitreal ranibizumab