EUCTR2021-000242-17-DK
Active, not recruiting
Phase 1
The effect of the popliteal plexus block on postoperative opioid consumption, pain, muscle strength and mobilization after total knee arthroplasty- a randomized, controlled, blinded study
Region Hospital Silkeborg0 sites165 target enrollmentJanuary 27, 2021
DrugsMarcaine
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Region Hospital Silkeborg
- Enrollment
- 165
- Status
- Active, not recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Scheduled to undergo primary total knee arthroplasty in spinal anesthesia
- •Able to perform a Timed Up and Go (TUG) test
- •Age \> 50 years old
- •Ability to give their written informed consent to participating in the study after having fully understood the contents of the study
- •American Society of Anesthesiologists (ASA) physical status 1, 2, or 3
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range 45
- •F.1\.3 Elderly (\>\=65 years) yes
Exclusion Criteria
- •Patients who cannot cooperate
- •Patients who cannot understand or speak Danish.
- •Patients with allergy or intolerance to the medicines used in the study
- •Patients with a daily intake of strong opioids (morphine, oxycodone, ketobemidone, methadone, fentanyl)
- •Patients suffering from alcohol and/or drug abuse – based on the investigator's assessment
- •Diagnosed with chronic central or peripheral neurodegenerative disorders
- •Body Mass Index \> 40
Outcomes
Primary Outcomes
Not specified
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