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Low-dose oxytocin combined with calcium for labor augmentation

Low-dose oxytocin combined with calcium versus low-dose oxytocin for labor augmentation: a randomised controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900025715
Enrollment
Unknown
Registered
2019-09-06
Start date
2019-08-30
Completion date
Unknown
Last updated
2019-10-28

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

Conditions

women need augmentation

Interventions

Sponsors

Guangzhou Women and Children Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Gestational weeks between 37 and 40+6 weeks; cephalic presentation; rupture of the membrane; spontaneous onset of labor; ineffective of uterine contraction.

Exclusion criteria

Exclusion criteria: scar uterus; cephalicpevic disproportion; significant bleeding during labor; III degree meconium amniotic fluid.

Design outcomes

Primary

MeasureTime frame
percentage of vaginal delivery;

Countries

China

Contacts

Public ContactYumian Lai

Guangzhou Women and Children Medical Center

lym7105@126.com+86 13533181763

Outcome results

None listed

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