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Trials / Unknown

UnknownNCT05682807

Effect of Caffeine Versus Probiotic on Preterm Neonates With Bronchopulmonary Dysplasia

Caffeine Versus Probiotic as Adjuvant Therapy for Preterm Neonates With Bronchopulmonary Dysplasia

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Tanta University · Academic / Other
Sex
All
Age
0 Weeks – 37 Weeks
Healthy volunteers
Not accepted

Summary

The aim of this study is to evaluate the effectiveness of caffeine versus probiotics supplementation as adjuvant therapy for preterm neonates with Bronchopulmonary dysplasia (BPD).

Conditions

Interventions

TypeNameDescription
DRUGCaffeine5-10 mg/kg/day IV maintenance dose given after 24 h for 2 months.
DRUGProbiotic Formulaprobiotics sachets supplementation orally, in the form of lyophilized lactic acid bacteria each Aluminium stick pack contains 100 mg ( Meyer et al., 2020) Probio Tec BB12-Blend 30- IF\* (SANDOZ®.) mixed with 10 ml sterile water and given by Ryle tube once daily until discharge from the unit after clinical and laboratory improvement after two months.

Timeline

Start date
2022-06-30
Primary completion
2024-06-01
Completion
2025-06-01
First posted
2023-01-12
Last updated
2023-01-12

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05682807. Inclusion in this directory is not an endorsement.

Effect of Caffeine Versus Probiotic on Preterm Neonates With Bronchopulmonary Dysplasia (NCT05682807) · Clinical Trials Directory