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Clinical and radiological results after MTP-1 revision arthrodesis

Clinical and radiological results after MTP-1 revision arthrodesis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00023636
Enrollment
62
Registered
2021-02-16
Start date
2019-02-22
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

M20.1 M20.2

Interventions

Group 1: Patients who underwent arthrodesis of the MTP-I joint using the anatomical angle-stable Medartis MTP-I arthrodesis plate with interposition of an autologous bone chip of the iliac crest in th

Sponsors

Medizinische Hochschule Hannover
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Arthrodesis of the MTP-I joint using the anatomical angle-stable Medartis MTP-I arthrodesis plate with interposition of an autologous bone chip of the iliac crest in the period January 2012 to February 2019 in the orthopedics department of the MHH at Diakovere Annastift. - In the control group MTP-I arthrodesis without bone chip grafting.

Exclusion criteria

Exclusion criteria: - Concomitant operations on the hindfoot, ankle or lower leg. These criteria also apply to the selection of control patients.

Design outcomes

Primary

MeasureTime frame
The primary objective of the planned study is to evaluate the rate of pseudarthrosis after performing MTP-I interposition arthrodesis using a new MTP-1 arthrodesis plate and compare it to a matched-pair patient population.

Secondary

MeasureTime frame
Secondarily, the time to bony healing is to be determined. In addition, the subjective result on the part of the patient and possible complications are recorded. A foot pressure measurement is used to assess the extent to which the operated toe can again participate in weight-bearing.

Countries

Germany

Contacts

Public ContactYvonne Noll

Orthopädische Klinik der Medizinischen Hochschule Hannover im Diakovere Annastift, Leitung Klinisches Studienmanagement

yvonne.noll@diakovere.de0511-5354-649

Outcome results

None listed

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