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Survey of biomechanical-functional and health economic parameters to assess the recovery of foot function after tibiotalar arthrodesis

Survey of biomechanical-functional and health economic parameters to assess the recovery of foot function after tibiotalar arthrodesis - Tibiotalar fusion

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00028256
Enrollment
60
Registered
2022-05-11
Start date
2022-09-12
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

M19.17

Interventions

Group 1: Patients with planned arthrodesis of the upper ankle are examined pre-operatively, as well as 6 and 12 months post-operatively. Various instrumental gait analysis procedures, scores, routine

Sponsors

BG Unfallklinik Murnau gGmbHInstitut für Biomechanik
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: - Symptomatic unilateral post-traumatic osteoarthritis of the upper ankle joint - Age 18 - 70 - Patient is able to understand the study procedure and has provided written informed consent

Exclusion criteria

Exclusion criteria: - Existing arthrodesis of the ipsi- and contralateral foot - Bilateral OSG arthrosis - symptomatic (subsequent) arthrosis of the ankles - Secondary gait disorder of neurological/internal or orthopedic origin (e.g. multiple sclerosis, herniated disc, coxarthrosis/gonarthrosis, knee/hip TEP, pelvic fractures, etc.) - Persons taking medication with known effects on the CNS - pregnancy - previous infection close to the joint (bony or soft tissue) - secondary arthritis (e.g. rheumatic) - primary or secondary foot deformities

Design outcomes

Primary

MeasureTime frame
Main outcome measures regarding the primary study hypothesis are the joint angles [°] at the affected leg between forefoot and hindfoot, hindfoot and tibia (definition according to Oxford Foot Model) and at the knee joint. In addition, the external ankle joint moments [Nm/kg] are analyzed. The data are collected using marker-based gait analysis.

Secondary

MeasureTime frame
- Postoperative satisfaction of the patient and foot function (SF-36, EQ-5D, AOFAS (modified)) - Type and extent of return-to-work (change in occupational activity after surgery, full-time/part-time activity) - Duration of incapacity for work - osseous reconstruction of the arthrodesis after 6 months (routine radiology) - Evaluation of the hindfoot angle achieved intraoperatively and its influence on outcome (preoperative and postoperative Saltzman imaging). - Detect possible predictors of healing progression from gait analysis data. - Survey of pain intensity and localization (NRS scale as part of the clinical examination in the gait laboratory). - Effect of surgical arthrodesis technique on consolidation rate.

Countries

Germany

Contacts

Public ContactIsabella Klöpfer-Krämer

BG Unfallklinik Murnau gGmbHInstitut für Biomechanik

ganglabor@bgu-murnau.de08841-48 4750

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026