Trials / Completed
CompletedNCT04094597
Safety and Efficacy of Oral Bovine Lactoferrin
Effectivness and Safety of Oral Bovine Lactoferrin in Neonatal Sepsis and Necrotizing Enterocolitis and Its Effect on Anaemia of Prematurity
- Status
- Completed
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- Cairo University · Academic / Other
- Sex
- All
- Age
- 1 Day – 7 Days
- Healthy volunteers
- Accepted
Summary
Oral lactoferrin versus Placebo will be given to preterm neonates
Detailed description
200 patient were included in the study , one hundred received oral placebo in the form of 2 ml saline , the other 100 preterm neonates received oral lactoferrin with monitoring of C-reactive protein , different cultures, complete blood count on day 7 and after one month.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lactoferrin | lactoferrin is given orally in comparsion to placebp |
| DRUG | Placebos | placebp is given in 2 ml saline |
Timeline
- Start date
- 2018-01-01
- Primary completion
- 2018-12-28
- Completion
- 2019-03-02
- First posted
- 2019-09-19
- Last updated
- 2019-09-19
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04094597. Inclusion in this directory is not an endorsement.