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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)

Phase 1
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 relief
MedDRA 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
Inclusion Criteria

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

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
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