Patent Ductus Arteriosus Clinical Trial
— SIMPLEOfficial title:
Can a New Scoring System Predict Hemodynamically Significant PDA Diagnosis and Treatment Requirement for Extremely Preterm Newborns Earlier
Patent ductus arteriosus (PDA) is an important morbidity of that the diagnosis and treatment is controversy in premature infants. A number of scoring systems have been developed, including the findings of echocardiography on the diagnosis and treatment of PDA. This study aimed to develop a new clinical scoring system that will enable the rapid, standard and noninvasive evaluation of hemodynamically significant PDA earlier, without relying on echocardiographic findings in premature babies with extremely low birth weight, and to determine the role of this scoring system in early diagnosis and treatment.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | February 15, 2021 |
Est. primary completion date | December 15, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A to 15 Days |
Eligibility |
Inclusion Criteria: - informed consent obtained from parents - extremely preterm infants - infants born before 28 gestational week Exclusion Criteria: - lack of informed consent - chromosomal abnormality - cardiovascular abnormality |
Country | Name | City | State |
---|---|---|---|
Turkey | Seda Yilmaz Semerci | Istanbul |
Lead Sponsor | Collaborator |
---|---|
Kanuni Sultan Suleyman Training and Research Hospital |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Participants with Patent Ductus Arteriosus | number of participants who diagnosed for hemodynamically significant PDA and had an elevated score of the newly developed system by us. | 7 days |
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