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Minimum Effective Volume of Lidocaine-Bupivacaine for Subgluteal Block

Minimum Effective Volume of Lidocaine-Bupivacaine for Ultrasound-Guided Subgluteal Sciatic Nerve Block

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02571699
Enrollment
60
Registered
2015-10-08
Start date
2016-03-31
Completion date
2016-12-31
Last updated
2016-06-13

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

Conditions

Injuries to the Ankle and Foot

Brief summary

The aim of this study is to determine the minimum effective volume of LA in 90 % of patients (MEV90) required for US-guided subgluteal sciatic nerve block.

Detailed description

The aim of this study is to determine the minimum effective volume of LA in 90 % of patients (MEV90) required for US-guided subgluteal sciatic nerve block. Success rate is defined as a minimal composite score of 6 points (out of 8 points) at 30 minutes.

Interventions

OTHERSubgluteal Nerve Block

ultrasound-guided subgluteal sciatic nerve block.

Sponsors

McGill University Health Centre/Research Institute of the McGill University Health Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* age between 18 and 75 years * American Society of Anesthesiologists classification 1-3 * body mass index between 20 and 35

Exclusion criteria

* adults who are unable to give their own consent * pre-existing neuropathy (assessed by history and physical examination) * coagulopathy (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. platelets≤ 100, International Normalized Ratio≥ 1.4 or partial prothrombin time ≥ 50) * renal failure (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. creatinine ≥ 100) * hepatic failure (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. transaminases ≥ 100) * allergy to LA * pregnancy * prior surgery in the subgluteal region * chronic pain syndromes requiring opioid intake at home

Design outcomes

Primary

MeasureTime frameDescription
success rate0-30 minutesminimal composite score of 6 out of 8 points

Countries

Canada

Contacts

Primary ContactMontrealGH

Outcome results

None listed

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