Comparison of Complication Rate, Functional Outcome and Quality of Life Between Standard Therapy … (NCT07199751) | Clinical Trial Compass
RecruitingNot Applicable
Comparison of Complication Rate, Functional Outcome and Quality of Life Between Standard Therapy Versus Fast-track Therapy in Patients Following Hip Replacement Surgery
Germany90 participantsStarted 2025-06-01
Plain-language summary
The fast track group vs. control group will be compared with regard to hospitalization time and the non-inferiority of the fast track group vs. control group with regard to HOOS will be assessed.
The questionnaires will only be collected in the study: Eq-5d-5l, HOOS, self-efficacy, enjoyment of movement, fear of movement, pain catastrophizing.
Who can participate
Age range
18 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:
* Age ≥18 years
* The patient will undergo surgery at Klinikum rechts der Isar, Technical University of Munich (TUM)
* Written informed consent for participation in the study after detailed explanation of the nature, significance, risks and scope of the clinical trial
* Written informed consent from the patient for data collection and data processing, with the patient fully informed.
* Sufficient German language skills of the patient.
Exclusion Criteria:
* Age \< 18 years
* The patient is under guardianship, legally incapacitated or has limited legal capacity
* Only partial weight-bearing permitted
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
Hospital length of stay (days)
Timeframe: From day of surgery until discharge, up to 4 days post-surgery
2
Hip Disability and Osteoarthritis Outcome Score (HOOS)
Timeframe: From baseline (pre-surgery) to 3 months post-surgery