Actively Recruiting

Phase Not Applicable
Age: 40Years - 75Years
All Genders
ID06641206

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

Age: 40Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients were not assigned for surgical intervention
  • Patients were free of exclusion criteria
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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

Loading map...

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Similar Trials

Comparison of Conventional and Cooled Radiofrequency Treatme...

Knee Osteoarthritis

Actively Recruiting

15 locations

A Pragmatic, Randomized Controlled Trial of a Auricular Poin...

Chronic Pain (Back / Neck)

Actively Recruiting

3 locations

Individual Differences in Gait and Osteoarthritis Pain

Knee Osteoarthritis (OA)

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here