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Clinical observation of the application of handheld ultrasound device in epidural anesthesia during cesarean section

Clinical observation of the application of handheld ultrasound device in epidural anesthesia during cesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048383
Enrollment
Unknown
Registered
2021-07-06
Start date
2021-07-10
Completion date
Unknown
Last updated
2022-03-14

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

Conditions

epidural anesthesia of cesarean section

Interventions

ultrasound group:ultrasonic location
control group:palpation location

Sponsors

Yantai Yuhuangding Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 22 to 45 years; 2.American Society of Anesthesiologists (ASA) classification I or III; 3.An elective cesarean section under spinal anesthesia was performed.

Exclusion criteria

Exclusion criteria: 1.Patients with central nervous system diseases, coagulopathy, skin ulceration and infection at the waist and back, and other contraindication of spinal anesthesia; 2.Spine malformation; 3.Patients have been injured or operated on their lower back; 4.Failure of puncture or change of anesthesia during operation.

Design outcomes

Primary

MeasureTime frame
Success at the first needle pass;Epidural depth estimation of handheld ultrasound device;

Secondary

MeasureTime frame
Puncture complications;The actual epidural depth;Patient satisfaction;Number of needle passes;Duration of the epidural procedure;

Countries

China

Contacts

Public ContactMa Jiahai

Yantai Yuhuangding Hospital

1317017141@qq.com+86 13656456186

Outcome results

None listed

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