Comparing Mulligan and Maitland techniques for knee osteoarthritis after PRP treatment
Comparative Effects of Mulligan and Maitland Techniques on Pain, Range of Motion and Functional Disability in Post Prp Knee Osteoarthritis
This study tests which physical therapy technique, Mulligan or Maitland, works better for people with knee osteoarthritis after they have received PRP treatment.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 36 (estimated) |
| Ages | 28 Years to 55 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Multan, Punjab) |
| Trial ID | NCT06460168 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of Mulligan and Maitland mobilization techniques in patients with knee osteoarthritis who have undergone platelet-rich plasma (PRP) therapy. The study involves a randomized design where participants aged 28-55 with grades 2 and 3 osteoarthritis are divided into two groups to receive either Mulligan or Maitland techniques. The primary outcomes measured include pain intensity, functional disability, and range of motion. The trial aims to determine which technique provides superior relief and improvement in knee function.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 28-55 with grade 2 or 3 knee osteoarthritis who have received PRP treatment.
Not a fit: Patients with grade 4 osteoarthritis, a history of knee surgery, or other joint conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide patients with more effective rehabilitation techniques for knee osteoarthritis, enhancing their quality of life.
How similar studies have performed: Previous studies have shown promising results with similar mobilization techniques in treating knee osteoarthritis, suggesting potential for success in this trial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age group 28-55 years * Male and female * Grade 2,3,4 of knee osteoarthritis * Post PRP Osteoarthritic knee joints included * After 1st month of Post PRP, patients will be included in study Exclusion Criteria: * History of surgery of the affected knee * Infection * Malignancy * Non Osteoarthritic joints excluded
Where this trial is running
Multan, Punjab
- Ibne Sina Hospital Multan — Multan, Punjab, Pakistan (Recruiting)
Study contacts
- Principal investigator: Muqaddas Shareef, DPT — Riphah International University
- Study coordinator: Imran Amjad, Phd
- Email: imran.amjad@riphah.edu.pk
- Phone: 03324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.