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NCT01049906 Clinical Trial

Popliteal Sciatic Nerve Block Catheter Placement for Foot Surgery

Foot Surgery Clinical Trial

Official title:
A Study to Determine the Quality of Sensory and Motor Blockade of Popliteal Sciatic Nerve Block Catheters Placed Under Ultrasound Guidance With and Without Nerve Stimulation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01049906
Other study ID # 07-008192
Secondary ID
Status Completed
Phase N/A
First received January 13, 2010
Last updated June 20, 2012
Start date October 2009
Est. completion date December 2011

Study information
Verified date June 2012
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Hypothesis: When performed under ultrasound guidance, there is improvement in the sensory and motor blockade obtained with stimulating popliteal catheters versus those placed without nerve stimulation.

Recruitment information / eligibility
Status Completed
Enrollment 21
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion criteria:

- patients scheduled to undergo foot or ankle surgery at Mayo Clinic Jacksonville

Exclusion criteria:

- emergency surgery

- peripheral neuropathy in the distribution of the sciatic nerve on the operative side

- history of recent alcohol or drug abuse

- allergy to local anesthetics

- pregnancy

- coagulopathy

- subjects declined to participate

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Intervention

Procedure:
• Placement of nerve block catheter
Placement of nerve block catheter with nerve stimulator and ultrasound
• Placement of nerve block catheter
Placement of nerve block catheter with ultrasound only

Locations
Country Name City State
United States Mayo Clinic in Florida Jacksonville Florida

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Complete motor and sensory anesthesia in the sciatic nerve distribution. Upon block placement No
See also
  Status Clinical Trial Phase
Completed NCT01229696 - Continuous Popliteal Nerve Blocks: Effect of Perineural Catheter Tip Location Relative to the Sciatic Nerve Bifurcation on Postoperative Analgesia Phase 4
Terminated NCT05354791 - Pre-post Spinal Popliteal Block
Terminated NCT01325012 - Ultrasound-Guided Continuous Sciatic Nerve Blocks: Popliteal Versus Subgluteal Catheters Phase 4
Enrolling by invitation NCT05425979 - Mepivacaine Versus Bupivacaine Onset Time in Ultrasound-guided Ankle Blocks Phase 4
Terminated NCT01615939 - A Study Comparing Continuous Sciatic Nerve Block to Single Shot Sciatic Nerve Block Phase 4
Enrolling by invitation NCT06465992 - Liposomal Bupivacaine With Dexamethasone for Foot Surgery Phase 4
Completed NCT05368012 - MIDCAB (Mid-Calf Block) for Foot Surgery Phase 4
Enrolling by invitation NCT04575688 - Periarticular Injection Versus Popliteal Block Phase 4
Recruiting NCT01546077 - Placement of Perineural Catheters in the Popliteal Region Phase 4
Recruiting NCT06309381 - Influence of Sensory Block Duration on Rebound Pain After Outpatient Foot Surgery Under Popliteal Sciatic Nerve Block.
Completed NCT04134962 - Evaluation of a New Tool for Measuring Hindfoot Alignment Under Load and in 3D.
Enrolling by invitation NCT04872322 - Effect of Ropivacaine During Popliteal Nerve Block in Foot and Ankle Surgery Phase 3