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Comparison of analgesic effects of two pudendal nerve block methods after maternal perineal incision

Comparison of analgesic effects of two pudendal nerve block methods after maternal perineal incision

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030404
Enrollment
Unknown
Registered
2020-03-01
Start date
2020-03-01
Completion date
Unknown
Last updated
2020-03-09

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

Conditions

Postoperative perineal pain

Interventions

Control group :Blinded pudendal nerve block

Sponsors

Department of Anesthesiology, the Second Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. 18 to 45-year-old women who have undergone vaginal delivery have undergone epidural analgesia and have stopped using epidural analgesia after childbirth; 2. The birth check is approved by the doctor in charge and there is no special inspection abnormality; 3. Perineal lateral incision for midwifery; 4. Requiring analgesia after perineal lateral incision and signing informed consent; 5. ASA grades 1-2 before anesthesia.

Exclusion criteria

Exclusion criteria: 1. People who are allergic to local anesthetics; 2. Childbirth under general anesthesia; 3. Perineal laceration during vaginal trial; 4. Hemorrhoids or other diseases that cause perineal pain before pregnancy; 5. Factors considered by anesthesiologists to cause difficulty in puncture or other risks after puncture: obesity, severe coagulation dysfunction, infection at puncture site, abnormal anatomy of puncture approach or other risks 6. The maternal physician or midwife believes that the mother has concerns about unsuitability to participate in the study, such as puerperal infection.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale/Score;

Secondary

MeasureTime frame
Incidence of adverse reactions;Time recording of pain onset;Discharge time;Postoperative discomfort;

Countries

China

Contacts

Public ContactCui Yulong

The Second Xiangya Hospital, Central South University

cuiyulong@csu.edu.cn+86 13974950203

Outcome results

None listed

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