Comparative study of labour analgesia onset with lidocaine for epidural technique versus bupivacaine for dural puncture epidural technique

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400092536

Enrollment

Unknown

Registered

2024-11-19

Start date

2024-11-25

Completion date

Unknown

Last updated

2024-12-02

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

Conditions

labor pain

Interventions

group DPE :the loading dose for initial labor analgesia is 20 ml of 0.1% bupivacaine combined with 0.3 µg/ml sufentanil.

group EP :the loading dose for initial labor analgesia is 20 ml of 0.57% lidocaine combined with 0.3 µg/ml sufentanil.

Eligibility

Sex/Gender

Female

Age

20 Years to 40 Years

Inclusion criteria

Inclusion criteria: single pregnancy,cephalic pregnancy,term (37-42 weeks), cervical dilation <5 cm,required labor analgesia

Exclusion criteria

Exclusion criteria: ASA>=?, pregnancy-related diseases (i.e.,gestational hypertension, gestational diabetes, preeclampsia), known fetal abnormalities, contraindications to neuraxial anaesthesia, Allergy to bupivacaine, lidocaine, or sufentanil.

Design outcomes

Primary

Measure	Time frame
The time for achieving "adequate analgesia" within 30 minutes after the completion of the injection of analgesic drugs;	—

Secondary

Measure	Time frame
The time from the puncture needle reaching the epidural space to achieving adequate analgesia;NRS ;sensory block level;	—

Countries

China

Contacts

Public ContactLiHong Sun

Women's Hospital, School of Medicine, Zhejiang University

sunlihong@zju.edu.cn+86 158 6901 2780

Outcome results

None listed

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