Computational Mathematical Analysis in Vastus Medialis Between a MTrP and Non Painful Point (NCT06514638) | Clinical Trial Compass
CompletedNot Applicable
Computational Mathematical Analysis in Vastus Medialis Between a MTrP and Non Painful Point
Spain66 participantsStarted 2023-11-13
Plain-language summary
With the help of ultrasound, the goal of the study is to asses the differences between MTR points and non painful points, in order to characterize the identification of MTR througought ultrasound. Being a complex process that needs to be standarized for each muscle, the study takes place in the vastus medialis.
Who can participate
Age range
18 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 18-65 year old.
* Presence of pain on palpation along the course of the muscle fibers of the vastus medialis of the quadriceps.
* Painful point and/or localized tense band with or without radiation of pain to the knee area or adductor region.
Exclusion Criteria:
* Serious diseases (neurological, psychiatric, systemic diseases, obesity).
* Knee or hip surgeries.
* Muscle tears in a state of recovery in the vastus medialis of the quadriceps.
* Inability to position yourself in a lateral decubitus position.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Echogenicity
Timeframe: Through study completion, an average of 3 months