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Effect of 12 weeks rehabilitation (aspect of neuromuscular physical therapy) in middle-aged patients in post-atroscopic period

Effect of 12 weeks rehabilitation (aspect of neuromuscular physical therapy) in middle-aged patients in post-atroscopic period

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2011-004087-30-EE
Enrollment
50
Registered
2011-08-22
Start date
2011-08-25
Completion date
Unknown
Last updated
2015-09-07

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

Conditions

Cartilage Lesion of the Knee Joint MedDRA version: 14.0 Level: LLT Classification code 10023476 Term: Knee osteoarthritis System Organ Class: 10028395 - Musculoskeletal and connective tissue disorders

Interventions

Trade Name: SonoVue Pharmaceutical Form: Dispersion for injection

Sponsors

Tartu University Department of Sports Medicine and Rehabilitation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Arthroscopy age 34-60 Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 50 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Contraindications to use of SonoVue

Design outcomes

Primary

MeasureTime frame
Main Objective: Assess the outcome of an exercise therapy (ExT) programme with longer duration (12 weeks) and higher intensity, focusing on the neuromuscular aspect in ExT.;Secondary Objective: * post-arthroscopy quality of life of the patient depends on the location and severity of cartilage damage *twelve-week neuromus¬cular ExT (nExT) has long term (12-month) effect on the patient’s quality of life. ;Primary end point(s): 1) knee-specific standardised questionnaire KOOS 2) range of motion of the hip and knee, 3) several performance tests of the lower limb ;Timepoint(s) of evaluation of this end point: The following parameters were measured in baseline and after the exercise therapy course 3 month after: 1) knee-specific standardised questionnaire KOOS 2) range of motion of the hip and knee, 3) several performance tests of the lower limb

Countries

Estonia

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026