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The Efficacy of Adductor-Canal-Blockade on Pain and Morphine Consumption After Revision Knee Arthroplasty

The Efficacy of Adductor-Canal-Blockade on Pain and Morphine Consumption After Revision Knee Arthroplasty

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01191593
Enrollment
36
Registered
2010-08-31
Start date
2010-09-30
Completion date
2013-04-30
Last updated
2013-08-22

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

Conditions

Knee Arthroplasty, Postoperative Pain

Keywords

Adductor-Canal-Blockade, postoperative pain, US-guided nerve block, revision knee arthroplasty

Brief summary

The purpose of this study is to determine whether Adductor-Canal-Blockade is effective at reducing pain and morphine consumption after revision knee arthroplasty.

Interventions

US-guided Adductor-Canal-Blockade with ropivacaine 7,5 mg/ml

US-guided Adductor-Canal-blockade with saline

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Revision Knee Arthroplasty in general anaesthesia * American society of anesthesiologists (ASA) 1-3 * BMI 18-40 * Written informed consent

Exclusion criteria

* Can not cooperate to the exam * Do not speak or understand Danish * Drug allergy * Alcohol or drug abuse

Design outcomes

Primary

MeasureTime frameDescription
Pain during 45 degrees active flexion of the knee4 hours postoperative0-100 mm at a visual analogue scale (VAS), at 4 hours postoperative.

Secondary

MeasureTime frameDescription
Pain during rest1-8 hours postoperative0-100 mm at a visual analogue scale (VAS), registered at the intervals 1, 2, 4, 6 and 8 hours postoperative, calculated as the area under the curve (AUC) for the interval 1-8 hours postoperative.
Total morphine consumption0-24 hours postoperativeTotal morphine consumption at the intervals 0-8, 8-24 and 0-24 hours postoperative.
Postoperative nausea1-8 hours postoperativeNausea scores(0-3)registered at 1,2,4,6 and 8 hours postoperative, calculated as mean value for the interval 1-8 hours postoperative.
Pain during 45 degrees active flexion of the knee1-8 hours postoperative0-100 mm at a visual analogue scale (VAS), registered at the intervals 1, 2, 4, 6 and 8 hours postoperative, calculated as the area under the curve (AUC) for the interval 1-8 hours postoperative.
Zofran consumption0-24 hours postoperativeTotal zofran consumption at the intervals 0-8, 8-24 and 0-24 hours postoperative.
Sedation1-8 hours postoperativeSedation score (0-3) registered at 1,2,4,6 and 8 hours postoperative, calculated as the mean value for the interval 1-8 hours postoperative.
Postoperative vomiting0-24 hours postoperativeNumber of vomiting episodes at the intervals 0-8, 8-24 and 0-24 hours postoperative.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026