Effekten af Adductor-Kanal-Blokade (AKB) på patienter efter rekonstruktion af forreste korsbånd (ACL) i dagkirurgisk regi(The Effect of Adductor-Channel Blockade (ACB) in Patients AfterAnterior Cruciate Ligament (ACL) Reconstruction in Daycase Surgery)
- Conditions
- Patients who have had a Reconstruction of the Anterior Cruciate Ligament. We want to investigate wheater Ropivacain can be used as a postoperative analgetic drug, when applied ultrasound-guided as a nerve block perineuraly around the saphenus nerve in the adductor canal. This could be an alternative method for postoperative analgesia with less side-effects than iv-administrated opioid/neuroaxial blockade.MedDRA version: 12.1Level: LLTClassification code 10036236Term: Postoperative pain reliefMedDRA version: 12.1Level: LLTClassification code 10054711Term: Postoperative pain
- Registration Number
- EUCTR2010-019517-16-DK
- Lead Sponsor
- Professor Jørgen B. Dahl
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 50
18-70 years of age
Surgery in general anesthesia (day-case surgery)
ASA-group I-II
BMI 19-35
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
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Patients who do not speak danish
Allergic reaktions toward drugs used in the trial
Abuse of alcohol/other drugs
Patients who can not be mobilised
Patients who can't cooperate (e.g dementia)
Pregnant women
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: Pain/VAS-score, patient standing, 2 hours postoperative;Secondary Objective: Pain/VAS-score at rest at different times<br>Pain/VAS-score standing/when mobilised, after 5 meters walk at different times<br>Postoperative pioid-consumption<br>Postoperative nausea/vomiting<br>Postoperative sedation<br>;Primary end point(s): VAS-score 2 hours post surgery, when standing
- Secondary Outcome Measures
Name Time Method