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Comparison of Two Techniques for Placement of Perineural Femoral Catheters.

Comparison of Ultrasound Hydrolocalization Technique Versus Neurostimulation for Placement of Continuous Femoral Catheters.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01726192
Acronym
HLOCSTIM2
Enrollment
50
Registered
2012-11-14
Start date
2012-08-31
Completion date
Unknown
Last updated
2012-11-14

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

Conditions

Anterior Cruciate Ligament Reconstruction, Postoperative Pain

Brief summary

The purpose of this study is to assess the efficacy of the hydrolocalization technique for placement of femoral perineural catheters in comparison with stimulating catheters. A non inferiority trial.

Detailed description

The investigators will randomize patients that will undergo anterior cruciate ligament reconstruction. Each patient will receive a subgluteal single shot nerve block and a continuous femoral nerve block with placement of a catheter either with the hydrolocalization technique (group HLOC) or a neurostimulating catheter (group NS).

Interventions

PROCEDUREPlacement of a femoral catheter with the hydrolocalization technique

Placement of femoral nerve catheter with the hydrolocalization technique, using ropivacaine 0.6%

PROCEDUREPlacement of a femoral neurostimulating catheter

Sponsors

Attikon Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* adults * BMI less than 30

Exclusion criteria

* known allergies to local anesthetics or other drugs used * patient refusal * any local or systemic contraindication to the use of popliteal block

Design outcomes

Primary

MeasureTime frame
local anesthetic consumption36 hours postoperatively

Secondary

MeasureTime frame
Pain scores with a VAS scale36 hours postoperatively

Other

MeasureTime frame
incidence of side effects, consumption of iv analgesics36 hours postoperatively

Countries

Greece, Italy

Contacts

Primary ContactTatiana F Sidiropoulou, MD, PhD
tatianasid@gmail.com00302105832371

Outcome results

None listed

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