KNEE ARTHROPLASTY USING DIGITAL TEMPLATING: A PROSPECTIVE RANDOMISED CONTROLLED SINGLE-BLIND TRIAL

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00021590

Enrollment

Registered

2020-04-30

Start date

2013-01-20

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

M17

Interventions

Group 1: Group A – study group – individual femoral valgus cut angle Group 2: Group B – control group – fixed femoral valgus cut angle = 7°

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: elective knee arthroplasty and the consent of the patient and surgeon to participate in the study

Exclusion criteria

Exclusion criteria: prior femur or tibia fracture, previous hip, knee or ankle bony surgery in anamnesis, knee joint varus or valgus deformity = 15° or flexion contracture > 10°, BMI = 40, and incorrect positioning on radiographs

Design outcomes

Primary

Measure	Time frame
femoral component absolute coronal angular deviation (FAD) and knee joint absolute coronal deformity (KAD) after the operation	—

Secondary

Measure	Time frame
Changes in clinical scores (pain NRS, KSS, KOOS) one year after the operation	—

Countries

Latvia

Contacts

Public ContactSergejs Zadoroznijs

Hospital of Traumatology and Orthopaedics / University of Latvia

sergejs.zadoroznijs@gmail.com+37167399400

Outcome results

None listed

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