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Neural Imaging for Patellofemoral Pain Syndrome
Study Summary
This trial looks at how knee pain affects movement in young women.
- Patellofemoral Pain Syndrome
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You have a medical condition or implant that makes it unsafe for you to have an MRI scan.A doctor has diagnosed you with knee pain in the front part of your knee, also known as patellofemoral pain or anterior knee pain.
- Group 1: Neural Imaging
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are there opportunities for participants to enroll in this experiment currently?
"Affirmative, according to the information provided by clinicaltrials.gov, this research endeavour is currently recruiting participants. It was initially advertised on November 16th 2017 and revised for the last time October 21st 2022. Two sites are enrolling a total of 30 individuals in the trial."
Does this research program take participants who are over the age of sixty?
"Eligibility for this research is limited to those aged between 7 and 40. In comparison, there are 378 studies that accept minors and 997 clinical trials available to seniors."
What is the scope of participants in this medical experiment?
"Affirmative. Clinicaltrials.gov's records demonstrate that this investigation is presently pursuing participants, having first been posted on November 16th 2017 and last updated October 21st 2022. The trial requires 30 individuals to be recruited from 2 distinct research centres."
What are the major goals of this medical experiment?
"The primary assessment of this two-year trial will be the Blood Oxygen Level Dependent (BOLD) Signal During Flexion/Extension Movement. Other secondary outcomes to track are scores from the International Knee Documentation Committee (IKDC) Subjective Knee Evaluation Form, Anterior Knee pain Scale (AKPS), and IKDC Questionnaire - all three measuring levels of perceived knee pain, function and disability."
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