Analysis of influencing factors of conversion to cesarean section in parturient with labor analgesia and its influence on maternal and infant outcomes

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200065784

Enrollment

Unknown

Registered

2022-11-15

Start date

2022-12-01

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

None listed

Interventions

cesarean group:None

control group:None

Eligibility

Sex/Gender

Female

Age

22 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade ?, aged 22-45 years; 2. Single fetus, 37-42 weeks gestation; 3. The woman consents voluntarily to a vaginal trial Labour, as assessed by an obstetrician, and epidural Labour analgesia, as assessed by an anesthesiologist.

Exclusion criteria

Exclusion criteria: 1. Gestational hypertension and gestational diabetes requiring drug control; 2. History of chronic pain or long-term use of analgesic drugs, contraindications to intraspinal anesthesia, history of neurological or psychiatric diseases; 3. Patients who are participating in other clinical studies; 4. Researchers consider other reasons unsuitable for clinical study.

Design outcomes

Primary

Measure	Time frame
Labor analgesia information;	—

Countries

China

Contacts

Public ContactChen Xinzhong

Women's Hospital, Zhejiang University School of Medicine

chenxinz@zju.edu.cn+86 13575738058

Outcome results