|

Effect of Honey Phonophoresis on Knee Cartilage Thickness

RECRUITINGN/ASponsored by University of Jazan
Actively Recruiting
PhaseN/A
SponsorUniversity of Jazan
Started2024-01-15
Est. completion2024-02-15
Eligibility
Age40 Years – 65 Years
Healthy vol.Accepted

Summary

Osteoarthritis (OA) is a progressive chronic disease with the loss of articular cartilage. It is now well recognized that the progression of the disease involves erosion of the cartilage, osteochondral inflammatory damage, and bone distortion. Many recent medical procedures provide treatment through improving symptoms through tissue regeneration and restoring homeostasis to local cells. Unlike bone, articular cartilage is rather recalcitrant to regenerate. Honey is a natural material contain 200 distinct chemical compounds in honey including a wide range of phenolic compounds that have antioxidant, bacteriostatic, antimicrobial, and anti-inflammatory properties. Honey was found to increase the printability and chondrogenic potential of a naturally derived bioink are the main formulations used as hydrogel for Articular Cartilage (AC) regeneration due to their similarity to chondral tissue in terms of morphological and mechanical properties. Design: Double blinded, Randomized control trial. Methods: 50 osteoarthritic patients will be evaluated to be allocated after they match the inclusion criteria then randomized to two groups, group A for Phonophoresis using Honey as coupling media with conventional physical therapy program, group B for ultrasound with regular gel as a coupling media with conventional physical therapy. Outcome measures: the primary outcome measure will be the thickness of the cartilage will be measured using diagnostic ultrasound, the secondary outcome measure will be knee pain measured by the visual analog scale (VAS) and Western Ontario and McMaster Universities OA Index (WOMAC) pain subscale, also functional mobility which will be measured using the stiffness and physical function subscales of the total WOMAC. All will be measured 1 day before starting the procedures and after 4 weeks of the intervention 3sessions/week.

Eligibility

Age: 40 Years – 65 YearsHealthy volunteers accepted
Inclusion Criteria:

* bilateral mild-to-moderate medial tibiofemoral Osteoarthritis

Exclusion Criteria:

1. rheumatologic conditions such as:

   * rheumatoid arthritis,
   * severe knee OA,
   * thrombosis of the lower limbs,
2. patients who had physiotherapy treatment of the knee in the previous 6 months,
3. a history of injections in the knee joint during the last 6 months,

   * balance disorders,
   * neuropathy or sensory disorders,
   * skin damage around the knee,
   * previous surgery on the knee joint, or a previous fracture of the lower extremity with knee joint involvement.
4. Patients will be also excluded if they have any contraindications or precautions for the use of ultrasound (e.g., infection, heart problems, pacemaker, metal implants, open epiphysis, pregnancy, thrombophlebitis, or impaired sensation)

Conditions2

ArthritisKnee Osteoarthritis

Browse More Trials

Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.