Trials / Terminated
TerminatedNCT03034733
The Effect of Dexamethasone on Pain After Total Knee Replacement Surgery
The Effect of Intravenous Single-dose Dexamethasone on Pain After Total Knee Replacement Surgery
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 27 (actual)
- Sponsor
- University of Oulu · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to examine, if a single-dose of dexamethasone given during the operation, alleviates pain after knee replacement surgery.
Detailed description
The purpose of this study is to examine, if a single-dose of dexamethasone given during the operation, alleviates pain after knee replacement surgery. This is also a dose-finding study comparing two doses of dexamethasone. Total knee arthroplasty causes considerable pain. Multimodal analgesia and peripheral nerve blocks are used for treatment of pain. Some studies suggest that glucocorticoids alleviate postoperative pain. The optimal dose of dexamethasone in treatment of postoperative pain is not known. Studies on this subject in patients with total knee replacement are sparse. Potential side-effects of dexamethasone (hyperglycemia, wound infection) need to be studied. Patients coming for primary knee replacement surgery are enrolled. The patients in each study group receive multimodal therapy for postoperative pain: etoricoxib, paracetamol, gabapentin and oxycodone. A single dose of intravenous dexamethasone (0,15 mg/kg or 0,25 mg/kg) or a placebo (saline) is administered to the patient during the operation. The effect of dexamethasone on postoperative pain is observed: main outcome is dynamic pain at 24 h postoperatively. The extent of inflammatory reaction is measured (CRP). Serial blood glucose measurements are done.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dexamethasone | intravenous dexamethasone, two groups: 0,15 mg/kg, 0,25 mg/kg |
| DRUG | Sodium Chloride, (24)NaCl 0,9% | intravenous placebo |
Timeline
- Start date
- 2017-02-15
- Primary completion
- 2018-01-31
- Completion
- 2018-01-31
- First posted
- 2017-01-27
- Last updated
- 2018-11-29
Locations
1 site across 1 country: Finland
Source: ClinicalTrials.gov record NCT03034733. Inclusion in this directory is not an endorsement.