Skip to content

Comparison of modified ultrasound-assistance and conventional landmark technique for mid-thoracic epidural placement: a randomized controlled trial

Comparison of modified ultrasound-assistance and conventional landmark technique for mid-thoracic epidural placement: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079729
Enrollment
Unknown
Registered
2024-01-10
Start date
2024-01-10
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

mid-thoracic epidural placement

Interventions

Ultrasound group:modified ultrasound-assisted technique using a stratified needle insertion site based on ultrasound images
Landmark Group:Using the conventional landmark technique

Sponsors

Department of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: a. Age = 18 years b. Scheduled for elective upper abdominal surgery or thoracic surgery and suitable for thoracic epidural analgesia c. Agree to use middle thoracic epidural analgesia d. Informed consent obtained

Exclusion criteria

Exclusion criteria: a. American Society of Anesthesiology physical status classification of V b. Contraindications to epidural catheterization c. Preexisting coagulopathy d. Localized infection e. Allergy to local anesthetics f. BMI > 30 kg / m2 g. Ppregnancy h. Patient refusal or failure to cooperate

Design outcomes

Primary

MeasureTime frame
first-pass success rate;

Secondary

MeasureTime frame
overall success rate;needling time;success at the first needle puncture;

Countries

China

Contacts

Public ContactYingXiao

Department of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China

xiaoying@mail.sysu.edu.cn+86 135 7052 1662

Outcome results

None listed

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