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Pregabalin for Osteoarthritis Pain

Phase 4
Waitlist Available
Led By Lee Kral, Pharm. D.
Research Sponsored by University of Iowa
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up approximately 6 weeks
Awards & highlights
Drug Has Already Been Approved
No Placebo-Only Group
Pivotal Trial

Summary

This trial tests if pregabalin can help reduce pain and improve function in patients with an overactive pain response undergoing knee replacement surgery. Pregabalin works by calming the nerves, making them less sensitive to pain. Pregabalin is a well-accepted treatment option for patients with nerve pain.

Who is the study for?
This trial is for people aged 50-85 with severe primary osteoarthritis needing knee replacement surgery, who are non-smokers for over two years and score at least 40 on the Central Sensitization Inventory. Excluded are those taking high doses of opioids, with poor kidney function, pregnant women or potential to become pregnant, prisoners, non-English speakers, suicidal individuals or current/recent users of pregabalin.
What is being tested?
The study tests if pregabalin can improve pain and function in patients with central sensitization undergoing total knee arthroplasty (TKA). Participants will either receive standard care or add pregabalin before and after surgery. They'll be monitored through physical therapy assessments and surveys about their pain levels and opioid use.
What are the potential side effects?
Possible side effects from pregabalin include dizziness, sleepiness, dry mouth, swelling in limbs, blurred vision, weight gain and difficulty concentrating. Patients will report any adverse effects they experience during the trial.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~approximately 6 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and approximately 6 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Calculate the Change Using the Knee Osteoarthritis Outcome Survey- Activities of Daily Living Subscale
Secondary study objectives
Calculate the Change Using the Knee Osteoarthritis Outcome Survey-Sports and Recreational Activities
Calculate the Change Using the Knee Osteoarthritis Outcome Survey-Stiffness
Calculate the Change Using the Knee Osteoarthritis Outcome Survey-Symptoms
+6 more

Awards & Highlights

Drug Has Already Been Approved
The FDA has already approved this drug, and is just seeking more data.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Study (Pregabalin)Experimental Treatment1 Intervention
Participants will receive pregabalin orally 75mg twice daily x 7 days prior to surgery, 150mg twice daily x 7 days after surgery, followed by 75mg twice daily x 7 days. Then Stop.
Group II: ControlActive Control1 Intervention
Participants will receive standard peri-operative pain management
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Pregabalin 75mg
2011
Completed Phase 4
~690

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Pregabalin, a common treatment for Central Sensitization Syndrome (CSS), works by modulating the release of neurotransmitters to reduce pain and central sensitization. This is particularly important for CSS patients because the condition involves an increased sensitivity of the central nervous system to pain stimuli. By decreasing the abnormal pain signaling, pregabalin helps alleviate the heightened pain response. Other treatments for CSS may include anticonvulsants and antidepressants, which also aim to modulate neurotransmitter activity and reduce central nervous system hyperactivity.
Pregabalin suppresses nociceptive behavior and central sensitization in a rat trigeminal neuropathic pain model.Pregabalin attenuates place escape/avoidance behavior in a rat model of spinal cord injury.

Find a Location

Who is running the clinical trial?

University of IowaLead Sponsor
465 Previous Clinical Trials
893,251 Total Patients Enrolled
Lee A. KralLead Sponsor
Lee Kral, Pharm. D.Principal InvestigatorUniversity of Iowa

Media Library

Pregabalin (Other) Clinical Trial Eligibility Overview. Trial Name: NCT05460871 — Phase 4
Central Sensitization Syndrome Research Study Groups: Control, Study (Pregabalin)
Central Sensitization Syndrome Clinical Trial 2023: Pregabalin Highlights & Side Effects. Trial Name: NCT05460871 — Phase 4
Pregabalin (Other) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05460871 — Phase 4
~7 spots leftby Nov 2025