Perineural Catheter Insertion Distance for Continuous Peripheral Nerve Blocks
- Conditions
- Lower Extremity SurgeryUpper Extremity SurgeryPost-operative Pain
- Interventions
- Procedure: Sciatic catheter left 0-1cm past needle tip vs. 5-6cm past needle tip
- Registration Number
- NCT00997867
- Lead Sponsor
- University of California, San Diego
- Brief Summary
This is a research study to determine if the effects of continuous peripheral nerve blocks are influenced by the distance of insertion past the needle tip of the perineural catheter.
- Detailed Description
Specific Aim: Research study to determine the relationships between perineural catheter insertion distance and subsequent continuous peripheral nerve block effects.
Hypothesis: during ultrasound-guided perineural catheter placement, inserting the catheter 0-1cm past the needle tip is associated with decreased postoperative pain compared with inserting the catheter 5-6cm past the needle tip.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 350
- undergoing surgery with a planned popliteal perineural catheter for postoperative analgesia
- age 18 years or older
- pregnancy
- inability to communicate with the investigators and hospital staff
- incarceration
- clinical neuropathy in the surgical extremity
- chronic high-dose opioid use
- history of opioid abuse
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Catheter 0-1cm past needle tip Sciatic catheter left 0-1cm past needle tip vs. 5-6cm past needle tip Patients will be receiving a sciatic (popliteal), femoral, or interscalene nerve block and will be randomized to having the catheter placed 0-1cm past the needle tip. The patient will be called the following day by research staff to assess their post-surgical pain. Catheter placed 5-6cm past needle tip Sciatic catheter left 0-1cm past needle tip vs. 5-6cm past needle tip Patients will be receiving a sciatic (popliteal), femoral, or interscalene nerve block and will be randomized to having the catheter placed 5-6cm past the needle tip. Patients will be called the following day by research staff to assess their post-surgical pain.
- Primary Outcome Measures
Name Time Method Average pain in the three hours previous to a phone call the day following surgery as measured on a numeric rating scale (0-10, 0=no pain, 10=worst imaginable pain). Day 1 after surgery, 3 hours prior to phone call
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
UCSD Medical Center
🇺🇸San Diego, California, United States