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Thai Baby Study Phase 1

National Situational Analysis of Birth Mode and Infant Outcomes in Thailand

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07498192
Enrollment
10300
Registered
2026-03-27
Start date
2026-03-01
Completion date
2026-12-31
Last updated
2026-03-27

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

Conditions

Outcome Assessment

Brief summary

The goal of this observational study is to examine national trends in mode of delivery and to assess associations between cesarean section and early-life health outcomes using routinely collected health data in Thailand. The study includes mother-infant dyads delivering in public hospitals across Thailand. The main questions it aims to answer are: Is cesarean delivery associated with increased risk of adverse neonatal outcomes compared with vaginal delivery? Is cesarean delivery associated with differences in early-life healthcare utilization and breastfeeding outcomes during the first year of life? Researchers will compare infants born by cesarean section with infants born by vaginal delivery to evaluate differences in neonatal morbidity, healthcare utilization, and breastfeeding patterns. Participants will not receive any intervention. The study involves secondary analysis of de-identified national health administrative and clinical data, including delivery records and linked maternal and infant health outcomes.

Interventions

None listed

Sponsors

Mead Johnson Nutrition
Lead SponsorINDUSTRY
Chulalongkorn University
CollaboratorOTHER
Ministry of Health, Thailand
CollaboratorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 120 Years
Healthy volunteers
Yes

Inclusion criteria

* Mother-infant dyads with delivery records available in the national health administrative database. * Deliveries occurring in public hospitals in Thailand during the study period. * Records containing information on mode of delivery and linked maternal and infant outcomes.

Exclusion criteria

* Records with missing or invalid delivery mode information. * Records that cannot be reliably linked between mother and infant.

Design outcomes

Primary

MeasureTime frameDescription
Neonatal health outcomes associated with mode of deliveryBirth to 28 days of lifeComparison of neonatal health outcomes, including birth asphyxia, neonatal infection, respiratory complications, and low birth weight, between infants born by cesarean section and vaginal delivery using routinely collected national health data.

Secondary

MeasureTime frameDescription
Early-life healthcare utilization during infancyBirth to 12 months of ageFrequency of healthcare utilization, including outpatient visits, emergency department visits, hospital admissions, and antibiotic use among infants by mode of delivery.
Breastfeeding outcomes by mode of deliveryBirth to 12 months of ageRates of exclusive and any breastfeeding among infants born by cesarean section compared with vaginal delivery, assessed using routinely collected health and nutrition records.
Temporal and geographic trends in cesarean delivery rates2015 to 2025Trends in cesarean section rates across regions, hospital levels, and time periods using national health administrative data.

Contacts

CONTACTJami Walker, MSc
jami.walker@reckitt.com812-429-7299
CONTACTAmber Jessell
amber.jessell@reckitt.com812-429-8903
STUDY_DIRECTORVeronica Fabrizio, DO

Mead Johnson Nutrition

PRINCIPAL_INVESTIGATORKrit Pongpirul, MD, MPH, PhD

Chulalongkorn University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026