Pain, Postoperative Clinical Trial
Official title:
Efficacy of Intravenous Dexamethasone Injection Given 12 and 24 Hours for Pain After Total Knee Arthroplasty: A Prospective Randomized Clinical Trial
The goal of this clinical trial is to investigate the efficacy of single dose and double dose of dexamethasone after primary total knee replacement. The main question[s] it aims to answer [is/are]: Does 24 hours-interval of double dose of dexamethasone have better analgesic effect than single dose and 12 hours interval of double dose of dexamethasone after primary total joint replacement? Researchers will compare double dose of dexamethasone group to see if [insert effects]. Participants will [describe the main tasks participants will be asked to do, interventions they'll be given and use bullets if it is more than 2 items].
Status | Recruiting |
Enrollment | 120 |
Est. completion date | October 31, 2025 |
Est. primary completion date | October 31, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 50 Years to 85 Years |
Eligibility | Inclusion Criteria: - Diagnosis of primary osteoarthritis of knee joint - Undergo unilateral primary total knee replacement - Age between 50-85 years old Exclusion Criteria: - Allergy to dexamethasone - History of long term corticosteroid used - New York heart association (NYHA) class > II - Type 2 Diabetes mellitus that had HbA1c > 7 % or FBS > 200 mg/dl - Chronic kidney disease > stage III or eGFR < 60 - Cirrhosis Child class B or C - Cannot use pain controlled as protocol - History of previous knee surgery - History of previous septic arthritis at knee joint |
Country | Name | City | State |
---|---|---|---|
Thailand | Thammasat University Hospital | Khlong Luang | Pathum Thani |
Lead Sponsor | Collaborator |
---|---|
Thammasat University Hospital |
Thailand,
Xu H, Zhang S, Xie J, Lei Y, Cao G, Pei F. Multiple Doses of Perioperative Dexamethasone Further Improve Clinical Outcomes After Total Knee Arthroplasty: A Prospective, Randomized, Controlled Study. J Arthroplasty. 2018 Nov;33(11):3448-3454. doi: 10.1016/j.arth.2018.06.031. Epub 2018 Jul 4. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain at rest and motion | Using visual analog scale 0-10 (0 means best, 10 means worst) | At 6 hour, 12 hour, 18 hour, 24 hour, 30 hour, 36 hour, 42 hour, 48 hour, 54 hour, 60 hour, 66 hour and 72 hour after surgery | |
Secondary | Nausea and vomiting | Using visual analog scale 0-10 (0 means best, 10 means worst) | At 24 hour, 48 hour and 72 hour after surgery | |
Secondary | Morphine consumption | Total milligrams use of morphine postoperative (record in mg) | At 24 hour, 48 hour and 72 hour after surgery | |
Secondary | Blood sugar level | record in mg/dL | At 24 hour and 48 hour after surgery | |
Secondary | CRP level | record in mg/dL | At 24 hour and 48 hour after surgery | |
Secondary | Range of motion | Using long arm goniometer (record in degrees) | At 24 hour and 48 hour after surgery | |
Secondary | Length of hospital stay | Number of days the patient stays for surgery | up to 1 week | |
Secondary | Complication | Surgical site infection, deep infection or wound complication | up to 6 months |
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