Effect of operation-anesthesia duration on neonatal outcome in obstetric general anesthesia

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1800016011

Enrollment

Unknown

Registered

2018-05-06

Start date

2018-06-01

Completion date

Unknown

Last updated

2018-05-14

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

Conditions

Delayed umbilical cord clamping

Interventions

None:None

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: pregnant women who were scheduled to undergo elective cesarean delivery for which general anesthesia had been decided on for clinical reasons

Exclusion criteria

Exclusion criteria: 1. gestational age less than 32 weeks; 2. fetal distress; 3. therapeutic regimen changed by the causes of pregnant women, such as respiration and circulation dysfunction, liver and renal dysfunction.

Design outcomes

Primary

Measure	Time frame
operation-anesthesia duration;cord artery blood gas analysis;Apgar score;	—

Secondary

Measure	Time frame
delivery room intubation; delivery room chest compressions;delivery room epinephrine;NICU admission;peak bilirubin;neonatal mortality;neonatal morbidities;	—

Countries

China

Contacts

Public ContactLi Huafeng

West China Second Hospital, Sichuan University

lihuafeng2005@hotmail.com+86 18180609219

Outcome results

None listed

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