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Controlling Femoral Extension and Derotation Osteotomy In Cerebral Palsy With Electromagnetic Tracking

Not Applicable
Conditions
Interal Rotation Gait
Malalignment
Crouch Gait
Cerebral Palsy
Interventions
Procedure: Femoral Extension and Derotation Osteotomy (ExtFDO)
Registration Number
NCT03528889
Lead Sponsor
Heidelberg University
Brief Summary

The study is designed to evaluate the use of electromagnetic tracking in multi plane femoral osteotomies, namely extension derotation osteotomies. The goal is to raise the precision of the surgical procedure in order to improve the outcome in short- and long term. All patients are examined with an instrumented 3D gait analysis pre- and one year postoperatively. The electromagnetic tracking system is evaluated against a base line CT or MRI scan serving as reference standard pre- and postoperatively.

Detailed Description

Internal rotation crouch gait is a common deformity in patients with spastic diplegia. The treatment includes soft tissue and bony correction. Especially the bony procedures e.g. femoral extension and derotation osteotomies have proven to be effective both in short term and long term evaluation. Nonetheless there is still a relevant number of patients that suffer from over- or under-correction and recurrence over time. The reasons are diverse and include false measurement of the amount of extension and/or derotation in OR.

The study now evaluates electromagnetic tracking for femoral extension and derotation to improve these results.

The patients are recruited from the outpatients department and included if they meet the criteria.

A baseline rotational CT or MRI scan and a 3D gait analysis are performed preoperatively. The patients are randomized into a electromagnetic tracking group or a classical goniometer group. The extension and derotation are measured with the EMT system or with a classic Moeltgen goniometer in the OR. Goal is to achieve the planned amounts of extension and derotation more accurately.

The surgical procedure follows standard rules and does not need alterations because of the study.

After the operation a second CT or MRI scan is performed and the extension and derotation are precisely evaluated by two raters and later compared to the results of the intraoperative electromagnetic tracking system. One year postoperative a second 3D gait analysis is performed to measure and compare the functional and dynamic outcome.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Cerebral palsy
  • GMFCS level I-III
  • Functionally disturbing internal rotation gait
  • Indication for femoral derotation osteotomy
Exclusion Criteria
  • No capacity of consent
  • Inability to perform all needed types examinations
  • Minors: Inability of getting a MRI rotational scan (i.e. pacemaker)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
EMTFemoral Extension and Derotation Osteotomy (ExtFDO)Extension FDO: procedure with electromagnetic tracking (EMT) controlling extension and derotation
GoniometerFemoral Extension and Derotation Osteotomy (ExtFDO)Extension FDO: classic procedure with goniometer controlled extension and derotation
Primary Outcome Measures
NameTimeMethod
Comparing the mean hip rotation between the groupsOne year after surgery

Measuring the functional outcome with the mean hip rotation comparing pre- and postoperative gait analysis of the patients.

Comparing the minimum knee flexion in stance phase between the groupsOne year after surgery

Measuring the functional outcome with the minimum knee flexion in stance phase comparing pre- and postoperative gait analysis of the patients.

Comparing the anterior pelvic tilt between the groupsOne year after surgery

Measuring the functional outcome with the anterior pelvic tilt comparing pre- and postoperative gait analysis of the patients.

Comparing the pelvic rotation between the groupsOne year after surgery

Measuring the functional outcome with the pelvic rotation comparing pre- and postoperative gait analysis of the patients.

Secondary Outcome Measures
NameTimeMethod
Evaluate the accuracy of bony derotation between the groupsShortly after surgery (not ore than 3 month) and again one year after surgery

Comparing the the planned amount of derotation in degrees with the intraoperative electromagnetic tracking values and the postoperative rotational MRI values in degrees to evaluate the accuracy of implementing a certain amount of bony derotation.

Comparing the bony derotation between the groupsShortly after surgery (not ore than 3 month) and again one year after surgery

Measuring the actual amount of derotation in degrees in a postoperative CT or MRI scan.

Evaluate the accuracy of bony extension between the groupsShortly after surgery (not ore than 3 month) and again one year after surgery

Comparing the the planned amount of extension in degrees with the intraoperative electromagnetic tracking values and the postoperative rotational MRI values in degrees to evaluate the accuracy of implementing a certain amount of bony extension.

Comparing the bony extension between the groupsShortly after surgery (not ore than 3 month) and again one year after surgery

Measuring the actual amount of extension in degrees in a postoperative CT or MRI scan.

Trial Locations

Locations (1)

Orthopedic Department, University of Heidelberg

🇩🇪

Heidelberg, Germany

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