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Effects of Low Dose Buprenorphine on Recovery After Hip or Knee Arthroplasty

Effects of Low Dose Buprenorphine on Recovery After Hip or Knee Arthroplasty

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02575664
Acronym
lonkkalaasta
Enrollment
160
Registered
2015-10-15
Start date
2012-08-31
Completion date
2015-10-31
Last updated
2015-12-29

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

Conditions

Osteoarthritis, Pain

Keywords

Pain, Arthroplasty, Buprenorphine

Brief summary

Buprenorphine is a highly lipophilic thebaine derivative that appears to have high affinity for mu-, kappa-, and delta-opioid receptors and low affinity for opioid receptors like 1 -receptors. It acts as a partial agonist at the mu-opioid and as a partial agonist/antagonist at the kappa-opioid, and as an antagonist at the delta opioid receptors. Buprenorphine has up to two-fold duration of action and it is approximately 30-fold more potent when compared to morphine. Pain is a common problem in patients coming to joint arthroplastic surgery. Buprenorphine low dose patches are recommended for treatment of moderate pain for example osteoarthritis pain. It is known that well treated pain even preoperatively may prevent prolonged postsurgical pain. In the present study the effects of low dose buprenorphine on postoperative pain and recovery were assessed.

Interventions

DRUGBuprenorphine

Buprenorphine 5 microg/h/7 days

DRUGPlacebo

Placebo patch

Sponsors

University of Eastern Finland
CollaboratorOTHER
Kuopio University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* no pregnancy/lactation, reliable contraception before menopause * elective knee or hip arthroplasty surgery * BMI (=body mass index) 18-35 kg/m2 * obtained informed consent

Exclusion criteria

* buprenorphine medication * allergy to study drugs• ikä \< 18 tai \>75 years * BMI \<18 tai\>35 kg/m2 * weight below 50 kg * Other contraindication for the study drug

Design outcomes

Primary

MeasureTime frameDescription
Pain relieftime from drug patch administration up to five weeksBrief pain inventory
Prolonged pain after arthroplastic surgeryfrom time from drug patch administration up to one yearBrief pain inventory

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026