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A study for the new 3D imaging ultrasound device in spinal anesthesia

A study for the new 3D imaging ultrasound device in spinal anesthesia: a prospective, single-center randomized controlled study.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031341
Enrollment
Unknown
Registered
2020-03-28
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-06-01

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

Conditions

spinal anesthesia

Interventions

experimental group:preprocedural scan using 3D imaging ultrasound device
control group:Traditional palpation positioning

Sponsors

Tongde Hospital of Zhejiang Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with age greater than or equal to 18 years old, ASA grade I~III, elective surgery with intravertebral anesthesia, signed informed consent.

Exclusion criteria

Exclusion criteria: Previous local anesthetic allergy, inability to cooperate with or any contraindications to spinal canal anesthesia (coagulation dysfunction, uncorrected insufficient blood volume, increased intracranial pressure or local skin infection), previous spinal surgery or serious spinal deformity.

Design outcomes

Primary

MeasureTime frame
Time taken for puncture;Total number of the puncture;—

Secondary

MeasureTime frame
The measured epidural depth;Actual epidural depth;The incidence of complications;Patient satisfaction;—

Countries

China

Contacts

Public ContactXie Shufang

Tongde Hospital of Zhejiang Province

xieshufang1991@163.com+86 13655814417

Outcome results

None listed

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