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Clinical research on the effects of different anesthesia methods on cesarean section anesthesia, maternal and infant outcomes, and the emotional state of parturients after failed painless delivery and their intervention

Clinical research on the effects of different anesthesia methods on cesarean section anesthesia, maternal and infant outcomes, and the emotional state of parturients after failed painless delivery and their intervention

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125694
Enrollment
Unknown
Registered
2026-05-29
Start date
2024-03-03
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Cesarean delivery

Interventions

Experimental Group:After confirming proper placement of the catheter in the epidural space without abnormalities, the experimental group received an intravenous bolus of 10ml of anesthetic solution (0
Control Group:The control group underwent subarachnoid block at the L3–4 interspace with administration of 2ml of 0.5% bupivacaine hydrochloride (10mg).
Subgroup E1:In subgroup E1, 10 mL of anesthetic mixture (0.375% ropivacaine hydrochloride combined with 1% lidocaine hydrochloride) was injected into the epidural space, and 5 mg dexamethasone was adm
Subgroup E2:In subgroup E2, 10 mL of anesthetic mixture (0.375% ropivacaine hydrochloride + 1% lidocaine hydrochloride) was injected into the epidural space, and no dexamethasone was administered intr
Subgroup C1:In subgroup C1, subarachnoid block was performed at the L3-4 interspace with 2 mL of 0.5% bupivacaine hydrochloride (10 mg) administered, and 5 mg dexamethasone was injected intravenously
Subgroup C2:In subgroup C2, subarachnoid block was performed at the L3-4 interspace with 2 mL of 0.5% bupivacaine hydrochloride (10 mg) administered, and no dexamethasone was given intravenously prior

Sponsors

Nanjing Jiangning Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Full-term primiparous women with a gestational age of 37–41 weeks who voluntarily request ELA; 2. ASA physical status ?–?, aged 22–40 years, body mass index (BMI) 20–35 kg/m², singleton cephalic presentation.

Exclusion criteria

Exclusion criteria: 1. Cases in which epidural analgesia fails and conversion to general anesthesia is required; 2. Cases requiring repeat puncture due to dislodgement of the epidural catheter; 3. Cases with failed subarachnoid puncture; 4. Fetuses complicated with intrauterine distress, developmental abnormalities or other conditions; 5. Subjects who refuse to participate in this study or cannot cooperate with postoperative follow-up.

Design outcomes

Primary

MeasureTime frame
Maternal Emotional Status Scales;Dosage of anesthetics and time required for parturients to meet surgical anesthesia requirements;Apgar scores of newborns at 1 and 5 minutes after birth; blood gas analysis indicators of umbilical artery immediately after delivery of newborns; fetal distress and neonatal asphyxia.;Maternal serum levels of stress hormones, pain mediators and inflammatory markers;

Secondary

MeasureTime frame
General vital signs of the parturients in the two groups were recorded respectively, including heart rate, pulse oxygen saturation, non-invasive blood pressure, etc.;Maternal adverse reactions;Routine blood test and biochemical indicators in parturients;

Countries

China

Contacts

Public ContactZhao Jun

Nanjing Jiangning Hospital

zhaojun_1986zj@163.com+86 137 7098 3755

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026