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Effect of dural puncture epidural versus standard epidural on onset time of anesthesia for cesarean section during labor analgesia

Effect of dural puncture epidural versus standard epidural on onset time of anesthesia for cesarean section during labor analgesia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089237
Enrollment
Unknown
Registered
2024-09-04
Start date
2024-09-20
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

Conversion from labor analgesia to cesarean section

Interventions

dural puncture epidural labor analgesia:In the DPE group,the neuraxial analgesia procedure was performed in the right lateral decubitus position at the L3–L4 interspace. The epidural space was accesse
epidural labor analgesia:In the EP Group, the neuraxial analgesia procedure was performed in the right lateral decubitus position at the L3–L4 interspace. The epidural space was accessed with a 17-gau

Sponsors

Obstetrics and gynecology Hospital of Tongji University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. ASA II; 2. Aged 18-45 years; 3. Gestational age greater than 37 weeks, healthy singleton pregnancies; 4. Primiparas undergoing labor analgesia via vaginal delivery.

Exclusion criteria

Exclusion criteria: 1.had contraindications to neuraxial anesthesia; 2.with combined systemic or chronic diseases; 3.severe fetal anomalies; 4.allergy to anystudy medications.; 5.other analgesics were used in the last 4 hours of labor

Design outcomes

Primary

MeasureTime frame
time from chloroprocaine administration to surgical anesthesia (T6 sensory blockade level);

Secondary

MeasureTime frame
quality of epidural anesthesia;the proportion of cesarean section;satisfaction;Pain score during surgery;opioid consumption within the first 24 hours;adverse events;vasopressors required;from primary outcome to start of surgery and duration of surgery ;

Countries

China

Contacts

Public ContactZhou Shuangqiong

Obstetrics and gynecology Hospital of Tongji University

zsq628628@163.com+86 139 1617 4158

Outcome results

None listed

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