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Correlation between oxytocin sensitivity and maternal and infant outcomes

Correlation between oxytocin sensitivity and maternal and infant outcomes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100047137
Enrollment
Unknown
Registered
2021-06-08
Start date
2021-06-07
Completion date
Unknown
Last updated
2022-01-24

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

Conditions

Oxytocin sensitivity and insensitivity

Interventions

Oxytocin sensitive group:None
Oxytocin insensitive group:None

Sponsors

Medical College of Nantong University (Nursing College)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Women with normal singleton pregnancies (>=28 gestational weeks); 2.Vaginal births in labor, absence of uterine contraction, and treatment with oxytocin infusion for labor induction.

Exclusion criteria

Exclusion criteria: 1.Aged < 18 years; 2.Maternal fever; 3.Known allergy to oxytocin treatment; 4.Fetal malformation, fetal distress, contracted pelvis, placenta previa, umbilical cord prolapse, transverse position; 5.Previous uterine rupture.

Design outcomes

Primary

MeasureTime frame
Apgar score;Umbilical cord blood pH;Postpartum hemorrhage;Turn of pediatrics;—

Secondary

MeasureTime frame
The first stage of labor;The second stage of labor;The third stage of labor;Forceps midwifery;—

Countries

China

Contacts

Public ContactZhang Feng

Medical College of Nantong University (Nursing College)

zhangfeng820909@163.com+86 13814715979

Outcome results

None listed

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