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CompletedNCT03746184TREATrightUpdated Sep 18, 2026

The Right Treatment for the Right Patient at the Right Time. A Study Following 5,000 Patients With Knee Osteoarthritis

An observational study in Knee Osteoarthritis, sponsored by Hvidovre University Hospital. Completed at 1 site in Denmark. Per ClinicalTrials.gov, last updated 2026-09-18.

Sponsored by Hvidovre University Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
3,507
Sex
All
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Study summary

The treatment that patients with knee OA are offered varies largely. There is a need for more evidence-based individualized guidance to treatment choice for knee osteoarthritis. This study will register and evaluate the course and outcome of treatment in 5,000 patients with knee osteoarthritis. The understanding of knee OA treatment will advance in three ways: Firstly, by describing the different treatment pathways that are currently being used for knee OA. Secondly, by identifying wich individual factors that may impact the outcome of the treatment course. And finally, by conducting the economic burden related to different treatment modalities.

Read the detailed description

The problem: Knee Osteoarthritis (OA), the most common form of arthritis, is a chronic, widespread disease with a steadily increasing prevalence that places a major economic burden on the society. Patients with knee OA suffer from chronic knee pain and functional disabilities. The treatment that patients with knee OA are offered varies largely, and is often not in coherence with clinical guidelines. The guidelines recommend patient education, exercise, and weight control as core interventions for all patients with knee OA and surgical intervention for end-stage knee OA. However, the timing of surgery is debated, and whether the outcome of different treatment strategies depend on individual factors such as the patients symptoms, OA severity, or prior treatment, has not been established.

The solution: This large-scale study aims at improving the understanding of which treatment should be offered to which patient with knee OA at which time. The study is an interdisciplinary, collaborative effort, including orthopaedic surgeons, physiotherapists and general practitioners from two different regions in Denmark. At least 5,000 patients with primary referrals to orthopaedic surgeons due to knee OA, at two public hospitals, will be recruited through a two-year inclusion period. Patients' prior treatment and symptom severity will be registered at the first consultation with the orthopaedic surgeon using a patient self-reported questionnaire. OA severity will be defined on plain standing knee radiographs using a well-established classification system. The course of treatment will be registered after 6 months and 2 years through a self-reported questionnaire with additional questions asking whether patients can accept their current symptom state, or, if not, whether they consider the treatment to have failed.

Societal impact and clinical implications: The understanding of knee OA treatment will advance in three ways: Firstly, our results will improve the overview by describing the different treatment pathways that are currently being used for knee OA. Secondly, predictors of good and poor treatment outcomes of different treatment modalities, or combinations hereof will be identified. And finally, the cost-effectiveness of different treatment modalities will be evaluated. These results will be used to develop a treatment algorithm to help patients with knee OA and clinicians to tailor the right treatment at the right time through shared decision-making.

02

Conditions studied

  • Knee Osteoarthritis

Keywords

  • precision medicine
  • Patient-Specific Modeling
03

In context

Osteoarthritis, Knee

3,302 studies on the registry are indexed under Osteoarthritis, Knee; 608 are open to participants now.

This study's enrollment of 3,507 is above the median of 100 across 472 observational studies indexed under Osteoarthritis, Knee.

Browse Osteoarthritis, Knee studies →

Lead sponsor

Hvidovre University Hospital is the lead sponsor of 295 studies on the registry; 21 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Sampling method
Non-probability sample

Study population

All patients with primary referrals to one of two public hospitals orthopedic department's outpatient clinics due to knee osteoarthritis are consecutively invited to participate. The two hospitals cover the larger part of Zealand in Denmark.

Inclusion criteria

  • primary referrals to one of two orthopedic department's outpatient clinics due to knee osteoarthritis

Exclusion criteria

Exclusion Criteria:

  • previous total or unicompartmental knee replacement
  • osteotomy around the study knee
  • unable to read or write Danish
  • patients who decline to answer the questionnaire at inclusion
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
3,507 participants (actual)
Target follow-up
2 Years
Patient registry
Yes

Groups and cohorts

  • Knee osteoarthritis

    Treatment course

    Other: Treatment course

Interventions

  • OtherTreatment course

    Pursued treatment for knee OA, including type of health care provider, time period of treatment course, and types of treatments received, will be recorded via the patient-reported questionnaire.

06

What researchers measure

Primary outcomes

  1. Patient Acceptable Symptom State (PASS)

    Patients answer yes/no to a PASS question asking whether they consider the current symptom state to be acceptable.

    Time frame: 2 years after inclusion

  2. Treatment Failure

    Patients who answer "no" to the PASS question will also answer "yes/no" to a question about whether they consider the treatment received to have failed.

    Time frame: 2 years after inclusion

Secondary outcomes

  1. Patient Acceptable Symptom State (PASS)

    Patients answer yes/no to a PASS question asking whether they consider the current symptom state to be acceptable.

    Time frame: 6 months after inclusion

  2. Treatment Failure

    Patients who answer "no" to the PASS question will also answer "yes/no" to a question about whether they consider the treatment received to have failed.

    Time frame: 6 months after inclusion

  3. Minimal Important Change

    An anchor question asking about the degree and importance of change in knee-pain and function will be answered on a 7-level Likert scale ranging from better, an important improvement to worse, an important deterioration.

    Time frame: 6 months and 2 years after inclusion

  4. Oxford Knee Score (OKS), range from 0 (worst) to 48 (best)

    Patient self-reported average knee pain and function during the past four weeks calculated from a validated 12-item questionnaire.

    Time frame: 6 months and 2 years after inclusion

07

Study locations

1 site
  • Department of Orthopaedic Surgery, Copenhagen University Hospital Hvidovre
    Hvidovre, 2650, Denmark
08

References and documents

Publications

  • Bruhn SM, Skou ST, Harris LK, Bandholm T, Moller A, Schroder HM, Troelsen A, Ingelsrud LH. Usage of guideline-adherent core treatments for knee osteoarthritis before and after consulting an orthopaedic surgeon: A prospective cohort study. Osteoarthr Cartil Open. 2023 Sep 28;5(4):100411. doi: 10.1016/j.ocarto.2023.100411. eCollection 2023 Dec. PubMed 37818279 ↗
  • Bruhn SM, Ingelsrud LH, Bandholm T, Skou ST, Schroder HM, Reventlow S, Moller A, Kjellberg J, Kallemose T, Troelsen A. Disentangling treatment pathways for knee osteoarthritis: a study protocol for the TREATright study including a prospective cohort study, a qualitative study and a cost-effectiveness study. BMJ Open. 2021 Jul 7;11(7):e048411. doi: 10.1136/bmjopen-2020-048411. PubMed 34233992 ↗

Individual participant data

Plan to share: Undecided — Decision in pending on whether the total database with all anonymised data will be transferred to the Danish National Archives' Collections once the study is completed.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03746184
Lead sponsor
Hvidovre University Hospital
Collaborators
Naestved Hospital, University of Copenhagen, VIVE - The Danish Center for Social Science Research, University of Southern Denmark
Responsible party
Anders Troelsen (Professor, consultant, dr.med., PhD, Hvidovre University Hospital) — Principal investigator
First posted
Nov 19, 2018
Start date
Oct 23, 2018
Primary completion
Apr 27, 2023
Completion
Apr 27, 2023
Last update
Sep 18, 2026

Study contacts

Anders Troelsen, Professor
study chair · Copenhagen University Hospital, Hvidovre
Lina H Ingelsrud, PhD
study chair · Copenhagen University Hospital, Hvidovre
Henrik M Schroeder, Asst. Prof.
study chair · Næstved Sygehus, Denmark
Søren T Skou, Assoc. Prof.
study chair · Næstved-Slagelse-Ringsted Hospitals AND University of Southern Denmark
Thomas Bandholm, Professor
study chair · University of Copenhagen AND Copenhagen University Hospital Hvidovre, Denmark
Jakob Kjellberg, Professor
study chair · VIVE - The Danish Centre of Applied Social Science, Denmark
Susanne Reventlow, Professor
study chair · University of Copenhagen
Anne Møller, Asst. Prof.
study chair · University of Copenhagen
Simon M Bruhn, M.Sc.
study chair · Copenhagen University Hospital, Hvidovre

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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