Transmucular Quadratus Lumborum Block: Potential Quadriceps Muscle Weakness
NCT05023343 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2021-12-21
Summary
The aim of this study is to examine whether the administration of the TQL block cause motor block of the lumbar plexus and thereby quadriceps muscle weakness. The investigators hypothesise that the administration of a unilateral TQL block does not cause quadriceps muscle weakness compared to a placebo block.
Conditions
- Neuromuscular Blockade
Interventions
- DRUG
-
Ropivacaine
30 mL Ropivacaine 0,75% administered as a unilateral TQL block
- OTHER
-
Quadriceps muscle strength
Quadriceps muscle strength is assessed using a hand-held dynamometer. Each participant is tested pre block administration and 60 minutes after
- OTHER
-
Timed Up and Go
To test mobilisation the standardised Timed Up and Go test is used. Each participant is tested pre block administration and 60 minutes after
- OTHER
-
Single-leg 6 meter timed hop test
To test muscle strength and power the single-leg 6 meter jump test is used. Each participant is tested pre block administration and 60 minutes after
- OTHER
-
Temperature discrimination
Dermatomal evaluation of cold and warm discrimination of the thoracic and lumbar dermatomes Approximately 60 minutes after block administration
- OTHER
-
Pinprick test
Dermatomal evaluation of pinprick/sharp sensation of the thoracic and lumbar dermatomes. Approximately 60 minutes after block administration
- DIAGNOSTIC_TEST
-
Blood samples
As a substudy the maximum serum concentration of ropivacaine is analyzed. Blood samples are taken at 0, 15, 30, 45 and 60 minutes after block administration
- DIAGNOSTIC_TEST
-
Non-invasive blood pressure measurement
Non-invasive blood pressure is measured prior to block administration and 30 minutes after block administration
Sponsors & Collaborators
-
Zealand University Hospital
lead OTHER
Principal Investigators
-
Katrine Tanggaard, MD · Zealand University Hospital, Department of Anaesthesiology
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-10-02
- Primary Completion
- 2021-11-28
- Completion
- 2021-11-28
Countries
- Denmark
Study Locations
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