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The Use of Ultrasound to Measure Depth of Thoracic Epidural Space

Use of Ultrasound to Measure Depth of Thoracic Epidural Space Compared With Blind Technique

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01172730
Enrollment
29
Registered
2010-07-30
Start date
2010-05-31
Completion date
Unknown
Last updated
2013-04-11

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

Conditions

Acute Pain, Post Operative Trauma

Keywords

Post operative pain, thoracic epidural, acute pain, Ultrasound scanning of the thoracic spine

Brief summary

The purpose of the study is to evaluate the use of ultrasound scanning of the thoracic spine to define the point of insertion and the depth of the epidural space compared to the blind technique. The study hypothesis is the use of Ultrasound will improve the success rate of epidural placement and may also decrease the rate of complications.

Interventions

Ultrasound scanning is used to define needle insertion point and depth of epidural space.

Sponsors

University of Massachusetts, Worcester
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients 18 years and older having a thoracic epidural catheter * Both male and female patients.

Exclusion criteria

* Pediatric population \< 18 years of age * Pregnancy * Prisoners * Absolute Contraindication to thoracic epidural placement severe scoliosis or deformity, * Patients with previous spine surgery or hardware implanted at level of epidural placement, * Anticipated ventilation postoperatively for a period more that 24 hrs * Lack of patient consent to enroll in the study

Design outcomes

Primary

MeasureTime frame
The success rate of epidural catheter to control painpost operative day # 1

Secondary

MeasureTime frame
The complication rate from epidural catheter placement.Immediate complications 24 hrs after

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026