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N/A N=140 Randomized Single-blind Treatment

Surgical or Exercise Therapy on Patients With Degenerative Meniscus Tears

Degenerative Meniscal Tear

Enrolled (actual)
140
Serious AEs
0.0%
Results posted
Jul 2024
Primary outcome: Primary: KOOS4 - Change From Baseline — 24.4; 25.3 units on a scale — p=<0.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Arthroscopic partial menisectomy (Procedure); Supervised neuromuscular and strength training (Other)
Age
Adult · 35+ yrs
Sex
All
Sponsor
Oslo University Hospital
Primary completion
Jul 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
KOOS4 - Change From Baseline
PRIMARY
Peak Torque Knee Extension - Change From Baseline
PRIMARY
Peak Torque Knee Flexion - Change From Baseline
PRIMARY
Knee Osteoarthritis Incidence
10; 9
PRIMARY
Radiographic Progression (the Osteoarthritis Research Society International [OARSI] Atlas) [Time Frame: At 10 Years]
SECONDARY
One Leg Hop Test - Change From Baseline
6.1; 11.0
SECONDARY
6 Meter Timed Hop Test - Change From Baseline
-0.3; -0.6
SECONDARY
Knee Bends 30 Sec - Change From Baseline
10.6; 9.2
SECONDARY
Peak Torque Knee Extension - Change From Baseline
SECONDARY
Peak Torque Knee Flexion - Change From Baseline
SECONDARY
One-leg Hop Test - Change in From Baseline
13.1; 13.2
SECONDARY
6 Meter Timed Hop Test - Change From Baseline
-0.3; -0.6
SECONDARY
Knee Bends 30 Sec - Change From Baseline
10.6; 9.2
SECONDARY
KOOS Pain - Change From Baseline
21.7; 23.2
SECONDARY
KOOS Symptoms - Change From Baseline
12.0; 17.4
SECONDARY
KOOS ADL - Change From Baseline
13.8; 15.4
SECONDARY
KOOS Sport/Rec - Change From Baseline
30.8; 29.3
SECONDARY
KOOS QOL - Change From Baseline
33.1; 31.3
SECONDARY
SF-36 MCS - Change From Baseline
-0.3; 1.1
SECONDARY
SF-36 PCS - Change From Baseline
7.0; 5.5
SECONDARY
KOOS Pain Subscale - Change From Baseline
SECONDARY
KOOS Symptoms Subscale - Change From Baseline
SECONDARY
KOOS ADL Subscale - Change From Baseline
SECONDARY
KOOS Sport/Rec Subscale - Change From Baseline
SECONDARY
KOOS QOL Subscale - Change From Baseline
SECONDARY
Peak Torque Knee Extension - Change From Baseline
SECONDARY
Peak Torque Knee Flexion - Change From Baseline
SECONDARY
Knee Osteoarthritis Incidence (Kellgren and Lawrence Classification )
SECONDARY
KOOS4 - Change From Baseline
SECONDARY
KOOS Pain Subscale - Change From Baseline
SECONDARY
KOOS Symptoms Subscale - Change From Baseline
SECONDARY
KOOS ADL Subscale - Change From Baseline
SECONDARY
KOOS Sport/Rec Subscale - Change From Baseline
SECONDARY
KOOS QOL Subscale - Change From Baseline
SECONDARY
Peak Torque Knee Flexion - Change From Baseline
SECONDARY
Peak Torque Knee Extension - Change From Baseline

Summary

This study is conducted as a collaboration between NAR, Orthopedic Department, Oslo University Hospital,Ullevaal, Hjelp24Nimi Oslo, Martina Hansens Hospital Norway, and University of Southern Denmark, Odense, Denmark. The investigators hypothesize that exercise is more effective than arthroscopic partial meniscectomy: a) on self-reported outcomes, functional performance and muscle strength in middle-aged patients subsequent to arthroscopic partial meniscectomy for a degenerative meniscus tear, and b) in preventing further development of knee osteoarthritis (OA).

Eligibility Criteria

Inclusion Criteria

  • Age 35-60 years
  • Knee pain for more than 2 months without a significant trauma
  • Medial meniscal tear on MRI
  • Eligible for arthroscopic partial meniscectomy
  • Grade 0-2 radiographic severity (specification after Kellgren Lawrence)

Exclusion Criteria

  • Those requiring acute trauma surgeries, including those treated as acute cases in the ER
  • Ligament injuries
  • Tumours (MRI)
  • Pain or other musculoskeletal comorbidities severely affecting lower extremity muscle function overriding the symptoms from the knee
  • Grade 3 or 4 radiographic severity (specification after Kellgren Lawrence)
  • Comorbidities excluding physical activities and exercise.
  • Previous knee surgery within two years
  • Not able to speak or read Norwegian, drug abuse or mental problems
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01002794). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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