Efficacy of Supplementing Oral Probiotics in Breastfeeding Mothers on Neonatal Weight

Efficacy of Supplementing Oral Probiotics to Breastfeeding Mothers on Neonatal Weight - nil

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/091827

Enrollment

102

Registered

2025-07-28

Start date

Unknown

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

None listed

Interventions

Intervention1: multistrain probiotic supplementation: multistrain probiotic supplementation to breastfeeding mothers as once daily dosing Intervention2: multistrain probiotic supplementation: multistr

Eligibility

Inclusion criteria

Inclusion criteria: Healthy breastfeeding mothers (aged 18 to 40 years) of Full term neonates with a birth weight of more than or equal to 2.5 kg. Exclusive breastfeeding commitment for at least one months.

Exclusion criteria

Exclusion criteria: Maternal antibiotic use within the last two weeks. Preterm neonates or those with congenital anomalies. Mothers with significant medical conditions (e.g., diabetes, hypothyroid, autoimmune diseases).

Design outcomes

Primary

Measure	Time frame
change in neonatal weight gainTimepoint: Baseline and 30 days.	—

Secondary

Measure	Time frame
To evaluate the effect of probiotics in preventing Neonatal Hyperbilirubinemia (NNH), and Necrotising Enterocolitis (NEC)Timepoint: 6 to 9 months	—

Countries

India

Contacts

Public ContactJaishree vasudevan

Chettinad Hospital and Research Institute

vsdvnjshr@gmail.com9444362134

Outcome results