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Adductor Canal Block and Effect of 10 Versus 30 ml Ropivacaine on Muscle Strength: a Randomized Study in Healthy Volunteers

Phase 4
Completed
Conditions
Muscle Strength
Healthy Volunteers
Interventions
Procedure: Adductor canal block with ropivacaine 0.1%
Registration Number
NCT01981746
Lead Sponsor
Rigshospitalet, Denmark
Brief Summary

To investigate whether reducing the volume (30 versus 10 ml) ropivacaine injected can reduce the number of subjects with impaired muscle strength following adductor canal block. We hypothesized that adductor canal block with 10 ml 0.1% ropivacaine preserves quadriceps strength compared with an adductor canal block with 30 ml.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
26
Inclusion Criteria
  • 18-30 years
  • Men
  • ASA 1
  • Body Mass Index 18-25
Exclusion Criteria
  • Allergy to study medication
  • Earlier trauma or surgery to the lower limb
  • Diabetes Mellitus

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
30 mlAdductor canal block with ropivacaine 0.1%30 ml ropivacaine 0.1%, single bolus
10 mlAdductor canal block with ropivacaine 0.1%10 ml 0.1% ropivacaine, single bolus
Primary Outcome Measures
NameTimeMethod
Number of subjects with reduced quadriceps strength0.5 to 6 hours post block

The difference between the two volumes in number of subjects experiencing a reduction in quadriceps muscle strength by more than 25% from baseline in two consecutive assessments.

Secondary Outcome Measures
NameTimeMethod
Quadriceps strength calculated as AUC30 minutes to 6 hours post block

The difference between the two volumes in maximum voluntary isometric contraction (MVIC) of the quadriceps muscle calculated as "area under the curve" (AUC)

Quadriceps strength in percentage of baseline2, 3 and 4 hours post block

The difference between the two volumes in maximum voluntary isometric contraction (MVIC) of the quadriceps muscle, assessed as percentage of the baseline value.

Modified 30-second Chair Stand test2 and 4 hours post block

The difference between the pre block value and the post block value in the modified 30-second Chair Stand test performed on one leg, between the two volumes.

VAS pain scores during warmth stimulationMean value for the periode 30 minutes - 6 hours post block

The difference between the two volumes in VAS pain score during warmth stimulation.

Trial Locations

Locations (1)

Department of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital, Rigshospitalet

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Copenhagen, Denmark

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