Application of real-time ultrasonic-guided epidural puncture in overweight parturient women and its effect on labor analgesia

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100042791

Enrollment

Unknown

Registered

2021-01-28

Start date

2021-01-28

Completion date

Unknown

Last updated

2021-05-10

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

Conditions

parturient women

Interventions

Group U:median approach use traditional method

Group P:paramedimedian approach use traditional method

Group UZ:median approach guilded by real-time ultrasound

Group UP:paramedimedian approach guilded by real-time ultrasound

Eligibility

Sex/Gender

Female

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: ASA grade II-III, 18-40 years old, gestational age were not less than 37 weeks, single pregnancy, BMI >= 30kg/m2.

Exclusion criteria

Exclusion criteria: Contraindication of epidural puncture, central nervous system disease, lumbar spine surgery or traumatic history, patients with scoliosis, refusal to cooperate or refused to participate in the study.

Design outcomes

Primary

Measure	Time frame
Accuracy of positioning intervertebral space;Number of times of puncture;puncture time;puncture time;Punctuation-related complications;	—

Countries

China

Contacts

Public ContactHe Mingfeng

Jiangsu Province Hospital

18551682286@126.com+86 18551682286

Outcome results

None listed

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