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Ultrasound-Guided Continuous Sciatic Nerve Blocks: Popliteal Versus Subgluteal Catheters

Ultrasound-Guided Continuous Sciatic Nerve Blocks: Popliteal Versus Subgluteal Catheters

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01325012
Enrollment
2
Registered
2011-03-29
Start date
2011-03-31
Completion date
2013-03-31
Last updated
2013-03-29

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

Conditions

Foot Surgery

Keywords

Pain, Surgery, Catheter, Nerve Block, Popliteal, Subgluteal, Sciatic, UCSD, Moderate-to-severe pain, Perineural Catheter, Orthopedic Surgery, foot surgery surgery, sciatic perineural catheter, age =>18

Brief summary

To determine the relationship between perineural catheter location along the sciatic nerve (popliteal versus subgluteal placement) and infusion effects for ultrasound-guided continuous sciatic nerve blocks.

Interventions

Patients randomized to this group will receive a sciatic nerve block with the catheter tip insertion at the subgluteal location 1-3 cm caudad to the inferior border of the gluteus maximus muscle. After catheter placement, outcome measures will be assessed.

Patients randomized to this group will receive a sciatic nerve block with the catheter tip insertion at the popliteal location 1-3 cm cephalad to the sciatic bifurcation. After Catheter placement outcome measures will be assessed.

Sponsors

University of California, San Diego
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* undergoing foot surgery with a sciatic perineural catheter for postoperative analgesia * spending the first postoperative night hospitalized * age 18 years or older

Exclusion criteria

* pregnancy * inability to communicate with the investigators and hospital staff * incarceration * clinical neuropathy in the surgical extremity

Design outcomes

Primary

MeasureTime frameDescription
Muscle Strength (MVIC) of the hamstring muscles08:00-09:00 morning after surgery as a percentage of baselineWe will evaluate hamstring strength which is innervated by the sciatic nerve with an isometric force electromechanical dynamometer to measure the force produced during a maximum voluntary isometric contraction (MVIC) in a seated position with the knees flexed at 90º

Secondary

MeasureTime frameDescription
Pain Scoresfrom leaving the PACU until 08:00 the morning after surgerySurgical pain scores both average and worse as collected by nursing staff; and also the average and worse pain during the primary endpoint measurement
Sleep Disturbancesrecorded at 08:00-09:00 the morning after surgery for the previous nightTotal number of times patient woke in the night due to surgical pain.
Sensory Effect08:00-09:00 morning after surgeryWe will evaluate tolerance of transcutaneous electrical stimulation. Electrocardiogram pads will be placed on the plantar and dorsal aspects of the foot, and attached to a nerve stimulator. The current will be increased from 0 mA until subjects described a buzzing sensation (not painful), at which time the current will be recorded as the tolerated level and the nerve stimulator turned off.
Anesthetic Leakagerecorded at 08:00-09:00 the morning following SurgeryLeakage from the catheter site noted by patient.
analgesic consumptionend of PACU stay until 08:00-09:00 the morning following surgeryHourly analgesic consumption.
Total Infusionrecorded at 08:00-09:00 the morning following SurgeryTotal infusiond duration in time and volume and total number of boluses delivered via catheter.

Countries

United States

Outcome results

None listed

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