Skip to content

The Mininimum Effective Anaesthetic Volume of Local Anaesthetic in Ultrasound-guided Shamrock Lumbar Plexus Block

The Mininimum Effective Anaesthetic Volume of Local Anaesthetic in Ultrasound-guided Shamrock Lumbar Plexus Block

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01956617
Enrollment
30
Registered
2013-10-08
Start date
2013-10-31
Completion date
Unknown
Last updated
2014-06-23

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

Conditions

Mininimum Effective Anaesthetic Volume of Local Anaesthetic

Brief summary

The Shamrock method is a new ultrasound-guided lumbar plexus block. The aim of the study is to determine the minimum effective volume of ropivacaine 0.5% required to produce an effective lumbar plexus block with this method. Using the Dixon and Massey up-and-down method study design, 30 patients scheduled for elective total hip and knee arthroplasty will be included in the study.

Interventions

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* orthopaedic patients scheduled for elective hip and knee arthoroplasty * ASA 1 - 2 or stable ASA 3 * age between 18 and 70 years * good ability to communicate and to cooperate

Exclusion criteria

* ASA \> 3 or unstable ASA 3 * BMI \> 32 * chronicle pain * nephrological diseases or nephropathy * known contraindications against the use of local anaesthetics * pregnancy

Design outcomes

Primary

MeasureTime frameDescription
minimum effective volumefrom day 1 up to 20 weeksThe primary outcome measure (MEV) is based on 30 measurements in 30 patients (secondary outcome measure: block success). MEV is determined by Dixon and Massey up-and-down method when all patients have been tested in the study

Secondary

MeasureTime frameDescription
block successDay 145 minutes after lumbar plexus blockade was performed

Countries

Norway

Outcome results

None listed

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