Overview

This trial is active, not recruiting.

Conditions pes plano valgus, flatfeet
Treatment lateral lengthening osteotomy of calcaneus
Sponsor University of Aarhus
Start date September 2010
End date October 2012
Trial size 10 participants
Trial identifier NCT01618812, M-20090162

Summary

In a group of children with severe and painful flatfeet lengthening procedures of calcaneus can be indicated. In this study the investigators use an artificial bone graft technique to avoid removing bone graft from the iliac crest.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective
Arm
Children with painful flatfeet
lateral lengthening osteotomy of calcaneus Hydroxyapatite
Use of artificial bone graft

Primary Outcomes

Measure
Healing of osteotomy
time frame: 104 weeks

Eligibility Criteria

Male or female participants from 8 years up to 20 years old.

Inclusion Criteria: - pain - gait disturbance Exclusion Criteria: - post traumatic conditions

Additional Information

Official title Calcaneal Neck Lengthening Osteotomy - Allogen Bone Graft Material Versus a Hydroxyapatite / β- Tricalcium Phosphate Bone Substitute
Principal investigator Martin Gottliebsen, PhD-student
Description The aim is to study the clinical and radiological effects of calcaneal lengthening with either autogen bonegraft or a HA-βTCP graft material in a group of children with planovalgus. The hypothesis is that it is possible to achieve a stabile osteotomy with HA-βTCP graft material equal to the use of autogen bonegraft thus avoiding the need to obtaining iliac crest graft material at growing children.
Trial information was received from ClinicalTrials.gov and was last updated in June 2012.
Information provided to ClinicalTrials.gov by University of Aarhus.