Clinical trial Recruiting at 1 site Observational Ages 18 and up

Standard recovery versus fast-track recovery after hip replacement surgery

Official title: Vergleich Der Komplikationsrate, Des Funktionellen Outcomes Und Der Lebensqualität Zwischen Standard Therapie Versus Fast Track Therapie Bei Patienten Und Patientinnen Nach Hüft-TEP Operationen

Run by Technical University of Munich · NCT07199751 · Data updated 2026-11-12

This project will test whether a fast-track recovery program helps adults after total hip replacement leave the hospital sooner while keeping similar function and quality of life compared with standard care.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment90 (estimated)
SponsorTechnical University of Munich
Academic / other
Locations1 site (München)
StatusRecruiting
StartedJune 1, 2025
Main results expectedDecember 31, 2025
Study endsDecember 31, 2025
Registry record updatedSeptember 30, 2025
Trial IDNCT07199751 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (age ≥18) scheduled for total hip arthroplasty at Klinikum rechts der Isar (TUM) who can give informed consent and speak sufficient German are ideal candidates.

Probably not a fit

Patients who require only partial weight-bearing, are under guardianship or legally incapacitated, or cannot attend follow-up at the Munich site are unlikely to be eligible or to benefit from the fast-track pathway.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational comparison at the Technical University of Munich comparing patients managed with a fast-track (enhanced recovery) pathway to patients receiving standard postoperative care after total hip arthroplasty. The main goals are to shorten hospital length of stay (targeting a reduction from about 6 to 4 days) and to show non-inferior functional outcome using the Hip disability and Osteoarthritis Outcome Score (HOOS). The study collects multiple patient-reported outcome measures (EQ-5D-5L, HOOS, self-efficacy, enjoyment of movement, kinesiophobia, pain catastrophizing) and objective measures (TUG, ROM, strength, pain NRS). Outcomes and complications will be compared between groups to determine whether faster discharge and earlier mobilization can be achieved without worse function or higher complication rates.

Why it matters

Potential benefit: If successful, the fast-track program could shorten hospital stays and speed recovery while maintaining function and quality of life.

How similar studies have gone: Enhanced recovery and fast-track programs for hip arthroplasty have been used widely and prior studies have commonly shown shorter hospital stays with comparable functional outcomes, so this work builds on existing evidence.

Who can join: the full rules

Show full inclusion / exclusion criteria
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

Where it's running

  • Department Physical Therapy
    München, Germany
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.