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
| Type | Name | Description |
|---|---|---|
| DRUG | Caffeine | 5-10 mg/kg/day IV maintenance dose given after 24 h for 2 months. |
| DRUG | Probiotic Formula | probiotics 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.