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

Controlling Femoral Extension and Derotation Osteotomy In Cerebral Palsy With Electromagnetic Tracking - A Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03528889
Enrollment
30
Registered
2018-05-18
Start date
2017-12-01
Completion date
2021-12-31
Last updated
2020-04-02

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

Conditions

Cerebral Palsy, Crouch Gait, Interal Rotation Gait, Malalignment

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.

Interventions

PROCEDUREFemoral Extension and Derotation Osteotomy (ExtFDO)

Correction of malrotation of the femoral bone and flexed knee gait by osteotomy, derotation and osteosynthesis

Sponsors

Else Kröner Fresenius Foundation
CollaboratorOTHER
Heidelberg University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Patients are masked about which group they are randomized in

Intervention model description

Randomization into two study arms: 1. Classic control of extension and derotation using a Moeltgen goniometer intraoperatively 2. Control of extension and derotation using an electromagnetic tracking device intraoperatively

Eligibility

Sex/Gender
ALL
Age
6 Years to 40 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Comparing the pelvic rotation between the groupsOne year after surgeryMeasuring the functional outcome with the pelvic rotation comparing pre- and postoperative gait analysis of the patients.
Comparing the mean hip rotation between the groupsOne year after surgeryMeasuring 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 surgeryMeasuring 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 surgeryMeasuring the functional outcome with the anterior pelvic tilt comparing pre- and postoperative gait analysis of the patients.

Secondary

MeasureTime frameDescription
Comparing the bony derotation between the groupsShortly after surgery (not ore than 3 month) and again one year after surgeryMeasuring the actual amount of derotation in degrees in a postoperative CT or MRI scan.
Comparing the bony extension between the groupsShortly after surgery (not ore than 3 month) and again one year after surgeryMeasuring the actual amount of extension in degrees in a postoperative CT or MRI scan.
Evaluate the accuracy of bony derotation between the groupsShortly after surgery (not ore than 3 month) and again one year after surgeryComparing 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.
Evaluate the accuracy of bony extension between the groupsShortly after surgery (not ore than 3 month) and again one year after surgeryComparing 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.

Countries

Germany

Contacts

Primary ContactThomas Dreher, Prof. Dr.
thomas.dreher@med.uni-heidelberg.de+4962215625000
Backup ContactMarco Götze, Dr.
marco.goetze@med.uni-heidelberg.de

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026