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Not yet recruiting NCT06920394

Functionality of Lower Limbs in Patients Who Have Undergone Knee Meniscectomy

Observational Meniscectomy Sequelae

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Survey using a questionnaire..
Who it may be relevant to
Registry conditions: Meniscectomy Sequelae. Basic parameters: 20 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Spain
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Functionality of Lower Limbs in Patients Who Have Undergone Knee Meniscectomy. A Multicenter Ambispective Cohort Study

Overview

Introduction. Meniscal lesions are common and are associated with the development of osteoarthritis of the knee. Work activities that cause mechanical stress can lead to acute or chronic injuries. The surgical treatment for this injury is meniscectomy. Physiotherapy is a widely accepted first-line treatment for patients with meniscus tears. Objective. To assess the clinical and functional status of patients who have undergone meniscus surgery with and without post-surgical physiotherapy. Material and method. Multicenter ambispective cohort study. 89 patients who have undergone meniscectomy will be recruited. The primary variable of the study will be functionality (Time Up \& Go), with the prescription of a post-surgical physiotherapy treatment being the dependent variable. The secondary variables, estimated as modifying or confounding, will be range of motion (goniometry), pain intensity (visual analog scale) and kinesiophobia (Tampa scale).

Interventions

  • Other Survey using a questionnaire.
    In the present study, no intervention will be carried out, and only the patients recruited will complete the questionnaires set out below.

Primary outcome measures

  • Assessment of knee functionality [Time frame: Screening visit]
Secondary outcome measures (3)
  • Assessment of range of knee motion [Time frame: Screening visit]
  • Assessment of pain perception [Time frame: Screening visit]
  • Assessment of Kinesiophobia [Time frame: Screening visit]

Eligibility criteria

Inclusion criteria

  • Persons aged 20 to 65
  • Of both sexes
  • With previous meniscectomy surgery in one of the two knees in the last 5 years
  • Who sign the informed consent document.

Exclusion criteria

  • Patients who require technical aids for walking
  • Dependent patients for carrying out activities of daily living
  • Patients over 65 years of age
  • Patients with cognitive impairments that prevent understanding of tests and evaluations

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Spain · 1 center
  • Universidad Católica San Antonio de Murcia — Murcia

Identifiers

NCT: NCT06920394 · FunctMenisc

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗