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This clinical trial will evaluate the effectiveness of platelet-rich plasma (PRP) injections for patients with anterior cruciate ligament (ACL) injury. ACL injuries commonly cause knee instability, pain, and reduced function, and rehabilitation alone may not fully restore recovery in all patients. PRP is prepared from a small sample of the patient's own blood and contains natural growth factors that may promote healing and improve joint function.
In this study, participants will be randomly assigned to one of two groups. The experimental group will receive a single ultrasound-guided injection of PRP into the knee joint along with a standard rehabilitation program. The control group will receive the rehabilitation program alone.
Participants will be followed up at 3 weeks, 8 weeks, and 16 weeks after treatment. At each follow-up visit, knee function, pain level, and physical performance will be assessed using validated outcome measures. The primary aim is to determine whether PRP provides additional benefit compared with rehabilitation alone in improving function and reducing symptoms in ACL-injured patients.
This study will provide new evidence about the role of PRP in ACL management, which may help guide future treatment decisions.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group A/Experimental group | Experimental | Will receive PRP and conventional conservative method (physical therapy, functional bracing, lifestyle modification) |
|
| Group B/Control group | Active Comparator | Will receive conventional conservative method (physical therapy, functional bracing, lifestyle modification) only |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| PRP injection | Biological | Ultrasound guided intraarticular PRP is given to the patient with partial ACL tear |
|
| Measure | Description | Time Frame |
|---|---|---|
| Visual Analog Scale (VAS ): Change in pain intensity measured by Visual Analog Scale | Pain intensity will be assessed using the Visual Analog Scale (0 = no pain, 10 = worst possible pain). | Baseline, 3 weeks, 8 weeks, and 16 weeks after intervention. |
| Measure | Description | Time Frame |
|---|---|---|
| KOOS: Change in functional outcome measured by Knee Injury and Osteoarthritis Outcome Score (KOOS) | KOOS assesses five domains: pain, symptoms, activities of daily living, sport/recreation function, and knee-related quality of life. | Baseline, 3 weeks, 8 weeks, and 16 weeks after intervention. |
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Inclusion criteria:
Exclusion criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Dr. Isfath Fauzia, MBBS | Contact | +8801744801604 | isfathfauzia20@gmail.com | |
| Prof. Dr. Md. Ali Emran, MBBS, FCPS | Contact | +8801716161616 | emran68@yahoo.com |
| Name | Affiliation | Role |
|---|---|---|
| Dr. Isfath Fauzia, MBBS | Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh | Principal Investigator |
| Prof. Dr. Md. Ali Emran, MBBS, FCPS | Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Bangabandhu Sheikh Mujib Medical University | Recruiting | Dhaka | 1000 | Bangladesh |
I will think later in case of mind change
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| conventional conservative method (physical therapy, functional bracing, lifestyle modification) | Other | conventional conservative method (physical therapy, functional bracing, lifestyle modification) |
|
|
| Dr. Md. Nuruzzaman Khandaker, MBBS, FCPS | Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh | Study Director |
| Dr. Md. Tariqul Islam, MBBS, FCPS | Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh | Study Director |
| ID | Term |
|---|---|
| D026741 | Physical Therapy Modalities |
| D012046 | Rehabilitation |
| ID | Term |
|---|---|
| D013812 | Therapeutics |
| D000359 | Aftercare |
| D003266 | Continuity of Patient Care |
| D005791 | Patient Care |
| D006296 | Health Services |
| D005159 | Health Care Facilities Workforce and Services |
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