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Femoral Cartilage Thickness In Patients With Lower Limb Amputation

I

Istanbul Physical Medicine Rehabilitation Training and Research Hospital

Status

Completed

Conditions

Amputation
Osteo Arthritis Knee

Study type

Observational

Funder types

Other

Identifiers

NCT04422717
IstanbulPMRTRH-HCK1

Details and patient eligibility

About

The aim of the study to investigate any relation with functional parameters and femoral cartilage thickness evaluation by ultrasonography in lower extremity amputate individuals.

Full description

In this prospective observational study, subjects approached Tertiary Rehabilitation Clinics for prothesis recipe or long term outpatient follow up was 150 people. Among them 76 subjects accepted to enroll study. Informed consent was taken. Subjects firstly performed clinical parameters at the first doctor's control. Knee radiography has been performed.

Enrollment

75 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being a single lower limb amputation
  • At least one year after the amputation operation
  • Prosthesis use for the last 6 months
  • Being traumatic or vascular
  • Not having stump infection
  • Muscle strength over stump should be at least 3/5

Exclusion criteria

  • Doing quadriceps exercise in the last 3 months
  • Trauma, surgery, and knee injections within 6 months (PRP, hyaluronic acid), Chondroitin-glucosamine use.

Being any of the active synovitides, Rheumatoid arthritis, spondyloarthritis, pseudogout, coxarthrosis, neuromuscular diseases

  • Having an additional disease that will cause psychiatric adjustment problem
  • Subjects are younger than 18 years
  • Bilateral amputated

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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