Acute Pain Clinical Trial
Official title:
Use of Ultrasound to Measure Depth of Thoracic Epidural Space Compared With Blind Technique
NCT number | NCT01172730 |
Other study ID # | 13495 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | May 24, 2010 |
Last updated | April 9, 2013 |
Start date | May 2010 |
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.
Status | Completed |
Enrollment | 29 |
Est. completion date | |
Est. primary completion date | April 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
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 |
Observational Model: Case-Only, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | UMass Memorial Medical Center | Worcester | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
University of Massachusetts, Worcester |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The success rate of epidural catheter to control pain | post operative day # 1 | Yes | |
Secondary | The complication rate from epidural catheter placement. | Immediate complications 24 hrs after | Yes |
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