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Comparison of dynamic versus static reconstruction of the medial patellofemoral ligament (MPFL)-a prospective study.

Comparison of dynamic versus static reconstruction of the medial patellofemoral ligament (MPFL)-a prospective study.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00031973
Enrollment
58
Registered
2023-06-01
Start date
2022-05-05
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

M22.0

Interventions

Group 1: In study center A (Orthopedic Clinic of the Hannover Medical School in the DIAKOVERE Annastift), patients are treated exclusively with dynamic MPFL reconstruction. Group 2: In study center B

Sponsors

Medizinische Hochschule Hannover
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patients with indication for MPFL reconstruction including possibly necessary cartilage therapies. - Age: >14 years

Exclusion criteria

Exclusion criteria: - Known hereditary connective tissue diseases (e.g. Ehlers-Danlos syndrome) - Known neuromuscular diseases - Significant other musculoskeletal diseases - Revision MPFL reconstruction - Concomitant procedures such as femoral and tibial realignment osteotomies, trochleoplasties and tuberosity transections - Trochlear dysplasia type C and D - TTTG distance > 20mm

Design outcomes

Primary

MeasureTime frame
The aim of the study is to demonstrate the non-inferiority of dynamic MPFL reconstruction against standard static MPFL reconstruction. Follow-up: 2 years Primary endpoint: Kujala score

Secondary

MeasureTime frame
Secondary endpoints: International Knee Documentation Committee (IKDC) score, Lysholm score, VAS, Tegner score, OR duration, material use, revision, re-dislocation.

Countries

Germany

Contacts

Public ContactYvonne Noll

Orthopädische Klinik der Medizinischen Hochschule Hannover

yvonne.noll@diakovere.de+49 511 5354 649

Outcome results

None listed

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