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Comparison of the onset time of 3% chlorprocaine, lidocaine carbonate, lidocaine carbonate + fentanyl in epidural anesthesia for Cesarean section

Comparison of the onset time of 3% chlorprocaine, lidocaine carbonate, lidocaine carbonate + fentanyl in epidural anesthesia for Cesarean section

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051195
Enrollment
Unknown
Registered
2021-09-15
Start date
2021-08-30
Completion date
Unknown
Last updated
2022-05-23

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

Conditions

Cesarean section anesthesia

Interventions

Group A:3% chlorprocaine
Group B:1.73% lidocaine carbonate
Group C:1.73% lidocaine carbonate + fentanyl

Sponsors

Affiliated Xiaoshan Hospital,Hangzhou Normal University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Maternal aged between 18 and 40 years; 2. ASA I or II level; 3. 150cm= 37 weeks.

Exclusion criteria

Exclusion criteria: 1. Spinal deformity; 2. Emergency cesarean section; 3. Twin and multiple pregnancy; 4. Communication barriers; 5. Refuse to sign the informed consent; 6. Coagulation disorders; 7. Infection at the puncture site.

Design outcomes

Primary

MeasureTime frame
The time from completion of injection to achievement of T6 sensory block to pinprick;The time from completion of injection to achievement of T8 sensory block to pinprick;

Secondary

MeasureTime frame
The number of cases of Hypotension;Bromage score;Neonatal Apgar score;The number of patients with pain. Pain, as defined by VAS score of three or more, with treated esketamine 0.3mg/kg intravenously.;

Countries

China

Contacts

Public ContactYu Jing

Affiliated Xiaoshan Hospital, Hangzhou Normal University

yujing985@163.com+86 18967168531

Outcome results

None listed

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