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Nonsteroidal Anti-inflammatory Drug
Celecoxib for Postoperative Knee Pain
N/A
Waitlist Available
Led By Adam Zanbilowicz, BA DPM MS
Research Sponsored by Zanbilowicz, Adam, DPM MS
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial seeks to determine if pre-operative anti-inflammatory therapy can help reduce postoperative pain in patients who have undergone knee arthroplasty surgery.
Who is the study for?
This trial is for healthy individuals scheduled for knee arthroplasty surgery. It's not suitable for those with heart disease, ulcers, bleeding disorders, liver disease with certain enzyme levels above normal, or impaired kidney function. Also excluded are patients on ACE inhibitors, diuretics, daily NSAIDs during the study period; pregnant women or those planning pregnancy soon; and anyone allergic to NSAIDs.Check my eligibility
What is being tested?
The study tests if taking Celecoxib (a painkiller that doesn't affect bleeding) for seven days before knee surgery can reduce postoperative pain by addressing inflammation. Participants will be randomly assigned to receive either Celecoxib or a placebo without knowing which one they're getting.See study design
What are the potential side effects?
While Celecoxib avoids issues with bleeding unlike other NSAIDs, potential side effects may include digestive problems like stomach upset or more rarely serious conditions such as heart problems and skin reactions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Compare total pain rating in group receiving 7day celecoxib against in 1 dose celecoxib
Secondary outcome measures
1. Comparison of pain rating VRS "When you woke up following surgery," and at 24 hours and 48 hours postoperatively in the two study groups
Comparison of patient reported maximum pain on VRS in the study groups.
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Who is running the clinical trial?
Zanbilowicz, Adam, DPM MSLead Sponsor
Adam Zanbilowicz, BA DPM MSPrincipal InvestigatorVancouver Coastal Health
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Eligibility Criteria:
This trial includes the following eligibility criteria:- My kidney function is not normal, with high creatinine levels.I am currently taking medication to help remove excess fluid from my body.You are allergic to non-steroidal anti-inflammatory drugs.I am currently taking another NSAID medication.I have a bleeding disorder.My liver enzymes are higher than normal.I will take an NSAID every day during the study.I have ulcers.I have heart disease.I am healthy and scheduled for knee replacement surgery.I am currently taking an ACE inhibitor medication.
Research Study Groups:
This trial has the following groups:Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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