- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05621785
Corticosteroid Use in Premature Babies and Lung Ultrasonografi Use in the Progression to Bronchopulmonary Dysplasia
The Effect of Postnatal Corticosteroid Use on Lung Ultrasonography Scores in Preventing the Development of Bronchopulmonary Dysplasia in Premature Infants
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
It is aimed to show the changes in lung ultrasound findings before, during and after steroid use in premature newborn babies born under 32/7 weeks. Thus, detailed new information will be obtained about the role and importance of corticosteroids in preventing the progression to BPD.
Postnatal corticosteroids are not routinely used to prevent BPD in our unit in our hospital. However, if premature babies meet the following criteria, postnatal low-dose corticosteroids are administered.
In the postnatal third week;
- Premature infants who are still not weaned from invasive mechanical ventilation.
- Those who continue to need non-invasive positive pressure ventilation
- Those who need more than 50% oxygen
Applied steroid protocols:
Dexomethasone:
Total cumulative dose 0.89 mg/kg
- 0.075 mg/kg/dose PO/IV (every 12 hours) for 3 days
- 0.05 mg/kg/dose PO/IV (every 12 hours) 3 days
- 0.025 mg/kg/dose PO/IV (every 12 hours) 2 days
- 0.01 mg/kg/dose PO/IV (every 12 hours) 2 days
Hydrocortisone:
- 1 mg/kg/dose IV/PO (every 12 hours) 7 days
- 0.5 mg/kg/dose IV/PO (every 12 hours) 3 days
Dexsometasone treatment is given in accordance with the DART protocol in infants who cannot wean from invasive mechanical ventilation in accordance with the protocols in use in our unit, which corticosteroid will be used. . In clinical follow-up, corticosteroid preference can be changed by the consultant neonatal specialist according to the general clinical condition of the patient and the accompanying spectrum. Which corticosteroid will be preferred in this observational study will not be known by the team that will conduct the study and will be recorded later.
If more than one corticosteroid use is required in the follow-up, pulmonary ultrasonography findings during the first corticosteroid use will be recorded.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Kırıkkale, Turkey, 71000
- Kırıkkale University Faculty of Medicine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Those who were born in Kırıkkale University Faculty of Medicine Hospital or who were born in other hospitals and were admitted to Kırıkkale University Faculty of Medicine Neonatal Intensive Care Unit within the first 48 hours of life.
- Gestational age below 32/7 weeks
- Those who will be administered postnatal corticosteroids with the decision of the consultant by meeting the diagnostic criteria for going to BPD
- Informed consent was obtained from the family
Exclusion Criteria:
- Those with cyanotic congenital heart disease
- Those with lung and thorax malformations,
- Those with major congenital anomalies
- Newborns who do not meet the criteria for postnatal corticosteroid therapy or who are not given postnatal corticosteroids by the consultant
- The family's refusal to give informed consent
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bronkopulmoner Displazi under the corticosteroid
Time Frame: 2 years
|
Although the use of corticosteroids in the course of BPD has a positive effect on lung ultrasound findings in the acute period in premature newborn babies, long-term beneficial effects cannot be observed.
|
2 years
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sevde Nur Vural, Asistant Dr, KIRIKKALE UNİVERSİTY FACULTY OF MEDİCİNE
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Kırıkkale University Faculty
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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