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Therapeutic effect of inhaled budesonide in transient tachypnea of newborn: A placebo-controlled study

Therapeutic effect of inhaled budesonide in transient tachypnea of newborn: A placebo-controlled study

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200513005
Enrollment
Unknown
Registered
2020-05-13
Start date
2016-06-29
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Transient Tachypnea of newborn tachypnea &#44

Interventions

inhalation of corticosteroids (budesonide 2 ml&#44
0.25 mg/ml suspension for nebulizer&#44
AstraZeneca AB&#44
Södertälje&#44
Sweden)&#44
the first dose was administered within 6 h of birth and the second dose was given 12 h later.,placebo
Experimental Drug,Placebo Comparator No treatment
inhaled budesonide,placebo

Sponsors

mohamed shawky elfarargy
Lead Sponsor
Ghada Alashmawy
Collaborator

Eligibility

Sex/Gender
All
Age
No minimum to 28 Days

Inclusion criteria

Inclusion criteria: full term neonates

Exclusion criteria

Exclusion criteria: preterm neonates

Design outcomes

Primary

MeasureTime frame
Transient Tachypnea of the newborn at 3 days after end of the intervention( inhaled budesonide) pulse oximeter to measure peripheral oxygen saturation

Secondary

MeasureTime frame
none none none

Countries

Egypt

Contacts

Public Contactmohamed elfarargy

Tanta University Hospital

farargy2009@hotmail.com00201005171750

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026