Instrumental Versus Standard Rehabilitation for Knee Osteoarthritis

Last updated: January 21, 2024
Sponsor: Mohammed V Souissi University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Osteoarthritis

Knee Injuries

Treatment

rehabilitation

Clinical Study ID

NCT06178380
knee osteoarthritis
  • All Genders

Study Summary

A randomized clinical trial to evaluate the effectiveness of an instrumental rehabilitation protocol compared with standard protocol In patients with knee osteoarthritis.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • patients with radiologically confirmed uni/ bilateral gonarthrosis

Exclusion

Exclusion Criteria:

  • Will be excluded from our study:
  • Subjects with congestive gonarthrosis (joint effusion at clinical examination).
  • Patients followed for chronic inflammatory rheumatism.
  • Patients who are candidates for surgery for knee osteoarthritis
  • Patients with a pathology causing a limitation in walking distance apart fromgonarthrosis.
  • Amputees of one or both lower limbs.

Study Design

Total Participants: 60
Treatment Group(s): 1
Primary Treatment: rehabilitation
Phase:
Study Start date:
July 01, 2021
Estimated Completion Date:
December 01, 2024

Study Description

This is a randomized clinical trial designed to compare two intervention aimed at reducing and improving knee function in patients with knee osteoarthritis

  • sixty subjects suffering from knee osteoarthritis will be recruited; 30 per group.

A: instrumental rehabilitation B:standard rehabilitation All patients who meet the clinical inclusion and exclusion criteria will have a standard radiography

  • selected patients will be invited to participate and will be informed of the purpose and conduct of the study

  • patients will be randomized to either the instrumental rehabilitation programme groupe or the standard rehabilitation group

  • patients in both groups will have a protocol that will be extended over 6 weeks

  • participants will be assessed primarily for function and pain, as well as other secondary endpoints , at baseline at 3 weeks and at 12 weeks.

Connect with a study center

  • Houda EL Moudane

    Rabat,
    Morocco

    Active - Recruiting

  • Houda EL Moudane

    Salé,
    Morocco

    Active - Recruiting

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