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Evaluation of AFO on knee OA

Evaluation of new ankle foot orthosis for patients with medial compartment osteoarthritis of the knee and Pilot study for evaluation of it’s effect on joint contact force, gait parameters, function, usability, pain and quality of life

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200516047459N7
Enrollment
10
Registered
2023-06-12
Start date
2023-06-22
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

knee osteoarthritis. Polyosteoarthritis, unspecified

Interventions

This pilot study will be conducted on ten patients with internal compartment osteoarthritis. Sampling will be done by easy non-random method and the subjects will be selected from the patients referre

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 50 years The severity of knee osteoarthritis be mild to moderate (grade 2 or 3) based on radiographic findings and the Kellgren-Lawrence scale Mild to moderate pain intensity (based on VAS scale, mild pain = 0-3, moderate pain = 4-6) Mild varus alignment in the knee with symptoms of osteoarthritis of the internal compartment of the knee Reporting of knee pain in most weekdays at least in the last month Not having movement restrictions in walking and standing Walking without any aids

Exclusion criteria

Exclusion criteria: History of knee replacement surgery History of lower limb fracture or knee ligament damage in the last year External compartment osteoarthritis (grade 1 and above) Having any cognitive or neurological disorder The patient is undergoing physiotherapy treatment or using other orthotic treatment

Design outcomes

Primary

MeasureTime frame
Force inside the knee joint. Timepoint: Before and six weeks later. Method of measurement: force plate.;Pain. Timepoint: Before and six weeks later. Method of measurement: Before and six weeks later.;Quality of life. Timepoint: Before and six weeks later. Method of measurement: Before and six weeks later.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoud Rafiaei

Esfahan University of Medical Sciences

ma.rafiaei@gmail.com+98 31 3792 5043

Outcome results

None listed

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