Less fluid, faster recovery? new study on newborn breathing trouble
NCT ID NCT07549945
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether giving less fluid to newborns with transient tachypnea (rapid breathing) helps them get better sooner. Fifty babies were randomly assigned to receive either restricted or standard fluid therapy. The main goals were to see how long they needed breathing support and how long they stayed in the hospital.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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50 people
The number who actually took part.
- Started
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Oct 2021
- Finished
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Jul 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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34 to 42 weeks
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Neonates born at our hospital with a gestational age of ≥34⁰/⁷ weeks who were diagnosed with TTN were included in the study. Exclusion Criteria: * Infants with severe congenital anomalies, those who required intubation in the delivery room or upon admission to the NICU, infants born through meconium-stained amniotic fluid, perinatally asphyxiated infants, infants with suspected sepsis based on risk factors or clinical findings, and infants diagnosed with TTN who did not require NIV were not included from the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hitit University Erol Olçok Training and Research Hospital
Çorum, Çorum, 19100, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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