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A randomized controlled trial for comparing sequential and simultaneous bilateral breast pumping for lactation initiation time and maintenance of lactation volume in postpartum non-immediate Breast-feeders

A randomized controlled trial for comparing sequential and simultaneous bilateral breast pumping for lactation initiation time and maintenance of lactation volume in postpartum non-immediate Breast-feeders

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018193
Enrollment
Unknown
Registered
2018-09-04
Start date
2018-03-01
Completion date
Unknown
Last updated
2018-09-10

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

Conditions

Breast-feeding

Interventions

Group 1:simultaneous breast pumping
Group 2:sequential electric breast pumping

Sponsors

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) mother with breastfeeding intention before delivery; (2) planned to express breast milk; (3) maternity leave =4 months; (4) maternal age between 20 and 40 years; (5) received prenatal breastfeeding education courses provided by the hospital; (6) delivered their infants =34 weeks gestational age and birth weight =2000 g or Cesarean section (including late preterm and term, twin and singleton deliveries); (7) Apgar score (1 min) =7 Note: late preterm account for 3/4 of preterm birth who are at increased risk of neonatal mortality and morbidity i.e., jaundice, poor feeding, respiratory distress, hypoglycaemia and sepsis[J Obstet Gynecol Neonatal Nurs 2011,40:9-24; BMC pediatrics 2016,16:179].

Exclusion criteria

Exclusion criteria: (1) contraindications to breastfeeding in mother, such as active or positive of infectious diseases, mentally retarded women and those receiving drugs or agents that will be harmful to breastfeeding infants; (2) mothers who had issues with alcohol use or smoke; (3) major deformed infants who may be defect in breastfeeding; (4) contraindications to breastfeeding in infants; (5) refusal of participation in this trial

Design outcomes

Primary

MeasureTime frame
Quantity of milking;First time of milking;

Secondary

MeasureTime frame
Milking methods;Pure breastfeeding duration;Rate of pure breastfeeding;

Countries

China

Contacts

Public ContactLin Zhang

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

zhanglin01@xinhuamed.com.cn+86 15821124166

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026