SENeGal SYNbiotic (SENGSYN) Study
- Conditions
- Digestive SystemNutritional, Metabolic, EndocrinePaediatrics
- Registration Number
- PACTR202102689928613
- Lead Sponsor
- iverpool School of Tropical Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other
- Sex
- All
- Target Recruitment
- 708
1) singleton newborn
2) birth weight (BW) or current weight (if BW not known) 2000g or more
3) well infant who is breastfed and has taken at least one breastfeed well
4) age 1-3 days
5) informed consent secured from mother/carer
6) Infants of HIV positive women without known immunosuppression
1) multiple pregnancy (e.g. twin/triplets)
2) suspicion or presence of any acute illness (e.g. fever, receiving treatment with antibiotics)
3) congenital abnormality that might be life-threatening or impair growth
4) infant with potential contraindication to synbiotic (e.g. suspected immune suppression; cardiac abnormality)
5) mother unlikely to stay in study area for the duration of the study
6) any health staff or study staff concerns regarding safety to participate in the trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method