Skip to content

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 After Anterior Cruciate Ligament (ACL) Reconstruction in Daycase Surgery)

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 After Anterior Cruciate Ligament (ACL) Reconstruction in Daycase Surgery)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2010-019517-16-DK
Enrollment
50
Registered
2010-03-26
Start date
2010-05-19
Completion date
Unknown
Last updated
2021-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

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: 12.1 Level: LLT Classification code 10036236 Term: Postoperative pain rel

Interventions

Trade Name: Naropin 7,5 mg/mL Product Name: Ropivacain Product Code: 17973 Pharmaceutical Form: Injection* INN or Proposed INN: ROPIVACAINE HYDROCHLORIDE CAS Number: 0 Concentration unit: mg/ml milli

Sponsors

Professor Jørgen B. Dahl
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Main Objective: Pain/VAS-score, patient standing, 2 hours postoperative;Secondary Objective: Pain/VAS-score at rest at different times Pain/VAS-score standing/when mobilised, after 5 meters walk at different times Postoperative pioid-consumption Postoperative nausea/vomiting Postoperative sedation ;Primary end point(s): VAS-score 2 hours post surgery, when standing

Countries

Denmark

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026