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The Impact of Scheduled Time Windows versus Conventional Timing for Elective Cesarean Delivery on Maternal and Neonatal Outcomes

The Impact of Scheduled Time Windows versus Conventional Timing for Elective Cesarean Delivery on Maternal and Neonatal Outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110895
Enrollment
Unknown
Registered
2025-10-22
Start date
2026-01-09
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Elective Cesarean Section

Interventions

Observation Group:None
Control group:None

Sponsors

The Second Nanning People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Single pregnancy, gestational age >= 37 weeks, elective cesarean section, pregnant woman/family member voluntarily requests a specific time, and there is no medical indication to perform surgery within a specific time.

Exclusion criteria

Exclusion criteria: Severe anemia;Thrombocytopenia;Poorly controlled hypertension;Poorly controlled hyperthyroidism;Poorly controlled diabetes mellitus;Immune system disorders;Heart disease;Voluntary withdrawal of informed consent;Conversion to emergency surgery prior to the procedure due to a medical indication;Intraoperative conversion to general anesthesia;Concurrent performance of myomectomy during the cesarean section;Occurrence of severe intraoperative complications (e.g., major hemorrhage, organ injury) necessitating a deviation from the original surgical plan;Failure to complete postoperative follow-up.

Design outcomes

Primary

MeasureTime frame
Perioperative Indicators: Surgery-related: Gestational age at delivery, indication for cesarean delivery, anesthesia type (neuraxial/general), incision-to-delivery (I-D) interval, total operative duration. Blood Management: Intraoperative blood loss (measured by weighing and volumetric method), postpartum hemorrhage (defined as blood loss =1000 ml), uterotonic usage (dose of carbetocin, methylergometrine, carboprost tromethamine), volume of crystalloid/colloid infusion (ml).;Postoperative Recovery Indicators: Complete blood count within 24 hours postoperatively (WBC, Hb, HCT, neutrophil percentage). Duration of postoperative antibiotic use. Postoperative hospital stay. Postoperative fever. Total hospitalization cost.;Neonatal Outcomes: Birth weight. Apgar score (1-min/5-min). Umbilical artery blood gas analysis (pH, BE, Lac; sampled within 1 minute after cord clamping). Neonatal hypoglycemia (blood glucose <2.6 mmol/L). NICU admission rate and indications.;

Secondary

MeasureTime frame
Maternal Baseline Data: Age, gravidity and parity, pre-pregnancy body mass index (BMI), pre-delivery BMI, gestational weight gain, gestational diabetes mellitus, hypertensive disorders of pregnancy.;

Countries

China

Contacts

Public ContactKaisun Zhao

The Second Nanning People's Hospital

339609234@qq.com+86 137 3708 5418

Outcome results

None listed

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