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Effect of different anesthesia modalities on neonatal cord blood pH, lactate values and neonatal outcome during emergency cesarean delivery

Effect of different anesthesia modalities on neonatal cord blood pH, lactate values and neonatal outcome during emergency cesarean delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104289
Enrollment
Unknown
Registered
2025-06-13
Start date
2025-06-25
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Emergency cesarean section

Interventions

Intrathecal anesthesia group:None

Sponsors

Nanjing Jiangning Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Gestational age >= 34 weeks, singleton pregnancy, emergency cesarean section (excluding elective surgery).

Exclusion criteria

Exclusion criteria: (1) Maternal-related confounding factors: Pregnancy complications: preeclampsia (systolic blood pressure >= 160 mmHg or proteinuria >= 5g/24h), gestational diabetes (abnormal OGTT and requiring insulin treatment); respiratory system diseases: COPD (GOLD classification >= II), acute asthma exacerbation (requiring bronchodilator treatment); circulatory system abnormalities: persistent hypotension (MAP 180 mmHg); hematological disorders: severe anemia (Hb 1.5 or platelets 95th percentile. (3) Labor-related interference factors: Abnormal labor: active phase arrest (cervical dilation stasis >= 4h), prolonged second stage of labor (primipara >3h / multipara >2h); obstetric interventions: emergency cesarean section (decision to delivery time = 3 times with abnormal fetal heart rate. (4) Drug interference factors: Oxytocin use: infusion rate >20 mU/min for more than 1 hour; tocolytics: prolonged intravenous administration of ritodrine, sublingual nitroglycerin; analgesics: non-study protocol opioids (pethidine >50 mg). (5) Specimen quality control: Improper timing of collection: non-standard blood collection time window (30-60 minutes after epidural administration); specimen handling defects: exposure to air for >2 minutes, failure to use heparinized collection tubes; testing delay: failure to conduct blood gas analysis within 15 minutes after blood collection.

Design outcomes

Primary

MeasureTime frame
Types of anesthetic drugs;Anesthetic drug dosage;Anesthesia operation time;Maternal hemodynamics;Umbilical cord blood pH;Cord blood lactate level;Apgar score for newborns;Neonatal resuscitation needs;Early complications;

Secondary

MeasureTime frame
Age;BMI;Comorbidities;Surgical urgency classification;

Countries

China

Contacts

Public ContactGuo Jidong

Nanjing Jiangning Hospital

gjd8606@163.com+86 25 5208 7000

Outcome results

None listed

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