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Arthroscopic Trochleaplasty in Chronic Relapsing Patellar Dislocations: A Follow-up Study

Evaluering av Kliniske Resultater Hos Pasienter Operert for Kronisk Residiverende Patellaluksasjoner Ved Hjelp av Artroskopisk Stabilisering Med Trokleaplastikk. En Kvalitetskontroll-studie

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06906419
Enrollment
20
Registered
2025-04-02
Start date
2025-05-01
Completion date
2025-12-31
Last updated
2025-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patellar Dislocation

Keywords

patellar dislocation, arthroscopic, trochleaplasty

Brief summary

This study aims to evaluate the long-term clinical outcomes of arthroscopic trochleoplasty in patients treated for chronic recurrent patellar dislocations. The primary objective is to assess the effectiveness of the procedure in reducing the need for re-operations and preventing recurrent instability. Secondary objectives include evaluating postoperative complications, patellofemoral pain, functional outcomes using the Kujala Anterior Knee Pain Scale (AKPS), and quality of life measured by EQ-5D-5L. This retrospective cohort study will analyze data from patient records and structured telephone interviews conducted at least one year post-surgery.

Interventions

None listed

Sponsors

Vestre Viken Hospital Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 18 years and older. * Underwent arthroscopic trochleoplasty for chronic recurrent patellar dislocations. * Surgery performed between 2015 and 2023. * Availability of follow-up data and consent for participation.

Exclusion criteria

* Concurrent knee surgeries unrelated to trochleoplasty. * Previous surgeries on the same knee. * Other significant orthopedic conditions affecting the knee. * Lack of follow-up data or consent.

Design outcomes

Primary

MeasureTime frameDescription
Re-operation RateThe investigators seek to register any re-operations from the time between the index surgery and the interview, ranging from 1 year up to 7 years postoperatively.Proportion of patients requiring additional surgical interventions after the index surgery at our institution.

Secondary

MeasureTime frameDescription
Postoperative ComplicationsThe investigators seek to register any complications related to the index surgery from the time between the index surgery and the interview, ranging from 1 year up to 7 years postoperatively.Frequency and type of complications following trochleoplasty.
Functional OutcomeAt the time of the interview, which will be performed from 1 year up to 7 years postoperatively.Kujala Anterior Knee Pain Scale (AKPS) scores assessing pain and knee function. The Kujala Score or Anterior Knee Pain Scale (AKPS) is a 13-item self-report questionnaire that assesses subjective reactions to particular activities and symptoms that are known to correlate with anterior knee pain syndrome. The AKPS is graded on a scale of 0 to 100, with 100 being the highest possible score. Lower scores reflect greater pain and disability.
Recurrent Instability RateThe investigators seek to register any incidences of recurrent instability from the time between the index surgery and the interview, ranging from 1 year up to 7 years postoperatively.Incidence of recurrent patellar dislocations post-surgery.
Pain AssessmentAt the time of the follow-up interview, which will be performed from 1 year up to 7 years postoperatively.Numeric pain rating scale (NRS), ranging from the least pain, 0, to the worst pain imaginable, 10, during daily activities.
Patient SatisfactionAt the time of the follow-up interview, which will be performed from 1 year up to 7 years postoperatively.Satisfaction score on a scale, ranging from 1 (very dissatisfied) to 5 (very satisfied).
EQ-5D-5L (HRQoL) scoresAt the time of the follow-up interview, which will be performed from 1 year up to 7 years postoperatively.EQ-5D-5L (HRQoL) scores evaluating general health and well-being. The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state.

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026