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Comparison results of the Kinematic and Mechanical align in the total knee arthroplasty

Comparison results of Kinematic align and Mechanical align knee arthroplasty in patients with osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201303286497N4
Enrollment
90
Registered
2015-07-24
Start date
2013-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Osteoarthritis. Osteophyte

Interventions

Intervention 1: Kinematic align Knee arthroplasty in the intervention Which is less soft tissue release. Intervention 2: Mechanical align knee arthroplasty in control group.
Treatment - Surgery
Treatment - Drugs
Kinematic align Knee arthroplasty in the intervention Which is less soft tissue release
Mechanical align knee arthroplasty in control group

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients diagnosed with Osteoarthritis of the knee joint with the informed consent Exclusion criteria: Patients who need blood transfusions before surgery; Bilateral knee surgery; Knee infection; Fracture during surgery were requiring fixation; Patients with charcot joint; Drug addict

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hemoglobin. Timepoint: Before and after surgery. Method of measurement: Recorded from File.;Days of hospitalization. Timepoint: post operation. Method of measurement: Questionnaire.;Pain. Timepoint: Post operation. Method of measurement: Visual Analg Scale.;Satisfaction. Timepoint: One year after operation. Method of measurement: Question of patient.;Time abandon the Waker and driving. Timepoint: One year after operation. Method of measurement: Question of patient.;Duration of surgery. Timepoint: Post operation. Method of measurement: Recorded from File.;Knee score. Timepoint: One year after surgery. Method of measurement: Lyshlom score.

Secondary

MeasureTime frame
Side effects. Timepoint: One year after surgery. Method of measurement: Recorded from file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahmood Karimi Mobarakeh

Kerman University of Medical Sciences

drkarimi_m@yahoo.com+98 34327229

Outcome results

None listed

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