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A NEW SCORING SYSTEM FOR PREDICTION OF PDA

Can a New Scoring System Predict Hemodynamically Significant PDA Diagnosis and Treatment Requirement for Extremely Preterm Newborns Earlier

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04270240
Acronym
SIMPLE
Enrollment
100
Registered
2020-02-17
Start date
2019-01-15
Completion date
2021-02-15
Last updated
2020-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patent Ductus Arteriosus, Prematurity; Extreme

Brief summary

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.

Detailed description

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.

Interventions

None listed

Sponsors

Kanuni Sultan Suleyman Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 15 Days
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants with Patent Ductus Arteriosus7 daysnumber of participants who diagnosed for hemodynamically significant PDA and had an elevated score of the newly developed system by us.

Countries

Turkey (Türkiye)

Contacts

Primary ContactSeda Y Semerci
sedayilmazsemerci@gmail.com05337180683
Backup ContactMerih Y Cetinkaya
drmerih@yahoo.com05337180683

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026