Actively Recruiting
Intra-articular Dexmedetomidine for Treatment of Chronic Knee Pain: A Prospective Case-Control Clinical Trial
Led by Tanta University · Updated on 2024-10-15
70
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Chronic knee osteoarthritis is a painful condition with limited treatment options that often reduce quality of life. Researchers are evaluating intra-articular dexmedetomidine, a sedative and pain-relief drug, as a new treatment for chronic knee pain. This prospective case-control clinical trial compares dexmedetomidine with other drugs to explore its potential benefits for managing pain in patients with chronic knee osteoarthritis. The study involves two groups of patients with chronic knee pain who have not received medical treatment and have decreased physical function and quality of life. One group receives dexmedetomidine injected into the knee joint, prepared as a 3 μg/kg dose in saline. The other groups receive active comparators: triamcinolone acetonide or bupivacaine hydrochloride injections. The study is randomized and double-blinded to fairly compare the treatments. Participants will be monitored for at least seven months after the injection. Researchers will assess pain levels using a numerical rating scale, focusing on the proportion of patients experiencing at least a 50% reduction in pain. The trial includes regular evaluations to measure pain relief and physical function, with safety monitored throughout the study period. The total participation time aligns with the follow-up duration to observe treatment effects.
CONDITIONS
Brief Title
Intra-Articular Dexmedetomidine: A Treatment for Chronic Knee Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients were not assigned for surgical intervention
- Patients were free of exclusion criteria
You will not qualify if you...
- Patients were assigned for surgical intervention
- Patients who had uncontrolled hypertension and/or diabetes mellitus
- Patients who had uncompensated cardiac, renal, or hepatic diseases
- Patients with coagulopathy, spinal deformity, allergy, or contraindication for the used drugs
- Patients who refused to sign the informed consent were excluded from the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 7 months
Participants receive intra-articular injections of dexmedetomidine, triamcinolone acetonide, or bupivacaine hydrochloride for chronic knee pain.
Trial Site Locations
Total: 1 location
1
Tanta University
Tanta, El Gharbyia, Egypt, 13511
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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