UnknownNot Applicable

Biplanar PSI Slope-reducing MOWHTO With Tibial Tuberosity Serving as Hinge Axis: Cadaveric Study

Poland6 participantsStarted 2022-06-22

Plain-language summary

Six cadaveric lower limbs will have PSI slope-reducing MOWHTO performed on and accuraccy of biplanar correction will be assessed.

Who can participate

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: Six fresh-frozen cadaveric lower limbs with 2/3 distal of femoral shaft and full-length leg with ankle and feet will be included in the study Exclusion Criteria: There will be no exclusion criteria for cadaveric lower limbs.

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

Feasibility of the 3D PSI device to achieve desired Medial Proximal Tibial Angle

Timeframe: Procedures will be perfomred on cadaveric limbs on 22th June 2022 and analyzed within 6 weeks

Feasibility of the 3D PSI device to achieve desired Medial Proximal Tibial Slope

Timeframe: Procedures will be perfomred on cadaveric limbs on 22th June 2022 and analyzed within 6 weeks

Feasibility of the 3D PSI device to achieve desired Lateral Proximal Tibial Slope

Timeframe: Procedures will be perfomred on cadaveric limbs on 22th June 2022 and analyzed within 6 weeks

Feasibility of the 3D PSI device to achieve desired anatomical FemoroTibial Angle

Timeframe: Procedures will be perfomred on cadaveric limbs on 22th June 2022 and analyzed within 6 weeks

Trial details

NCT IDNCT05448742

SponsorArtromedical Konrad Malinowski Clinic

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-31

View on ClinicalTrials.gov More Knee Disease trials