A NEW SCORING SYSTEM FOR PREDICTION OF PDA

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Patent ductus arteriosus
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Brief Title

A NEW SCORING SYSTEM FOR PREDICTION OF PDA

Official Title

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

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.

Study Type

Observational

Primary Outcome

Number of Participants with Patent Ductus Arteriosus

Condition

Patent Ductus Arteriosus

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Estimated Enrollment

100

Start Date

January 15, 2019

Completion Date

February 15, 2021

Primary Completion Date

December 15, 2020

Eligibility Criteria

        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

Gender

All

Ages

N/A - 15 Days

Accepts Healthy Volunteers

No

Contacts

, 05337180683, [email protected]

Location Countries

Turkey

Location Countries

Turkey

Administrative Informations

NCT ID

NCT04270240

Organization ID

MAEEAH6725

Responsible Party

Principal Investigator

Study Sponsor

Kanuni Sultan Suleyman Training and Research Hospital

Study Sponsor

, ,

Verification Date

May 2020