4 Dimensional - Impairment of Posttraumatic Forearm Rotation Evaluated With Computed Tomography

Pronation-Supination of the Forearm, Impairment of Clinical Trial

— 4D-IRECT  

Official title:

4 Dimensional - Impairment of Posttraumatic Forearm Rotation Evaluated With Computed Tomography : 4D-IRECT Pilot Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04067232
• Other study ID #: RECHMPL18_0463
• Secondary ID: UF 7729
• Status: Completed
• Phase: N/A
• Start date: January 16, 2020
• Est. completion date: June 15, 2020

Study information

• Verified date: September 2020
• Source: University Hospital, Montpellier
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study is to develop a 4D-CT (4 Dimensional Computed Tomography) -scan acquisition method for estimating the cause of posttraumatic impairment of the forearm. Both forearms of patients with posttraumatic impairment of one of the forearm will be scanned using a 4D-CT-scan, during forearm rotation. Rotation of impaired and healthy forearms will be analysed and compared to each other. This method is intended to allow differentiation of motion patterns reflecting an osseous impairment from those caused by soft tissue pathology in order to improve treatment choice.

Description:

Forearm and wrist fractures are the most common of all fractures and mostly occur at the distal end of the radius. Distal radius fractures are associated with posttraumatic sequelae, which typically involve restricted forearm rotation. Diagnostics of dynamic traumatic pathologies are conventionally based on static (2D or 3D) imaging protocols using MRI (magnetic resonance imaging) or CT. However, interpretation of indirect suggestive findings - such as edema or abnormal bone positions - limits accuracy and inter-observer reliability. Dynamic 4D imaging (adding the fourth dimension of time) has the potential to discriminate whether forearm rotation deficit is due to an osseous deformity causing bony impingement or whether it is due to non-osseous pathology. Hence it may reduce unnecessary corrective osteotomies and guide the patient and surgeon towards the most effective surgical or conservative treatment choice - expectedly resulting in better outcomes and patient satisfaction. In addition, we aim to develop a classification based on the estimated motion patterns and assess its reliability. Furthermore we aim at acquiring knowledge of physiological mechanics of the radioulnar joint and to assess symmetry in radioulnar joint motions between two healthy forearms on 4D-CT-scans.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: June 15, 2020
• Est. primary completion date: June 15, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with a one-sided posttraumatic impairment of forearm pro- and/or supination at least 3 months after injury

• Patients are above 18 years

• Patients who are willing to give informed consent

• National health insurance cover

Exclusion Criteria:

• A history of trauma to both forearms

• Any shoulder pathology or impairment preventing forward elevation of the arm as required during the scanning protocol

• Neuromuscular pathology

• Not able to understand or give informed consent

• Pregnancy (ßHCG positive), breast-feeding or the absence of effective contraception for women of child-bearing age

• Legal incapacity (persons in custody or under guardianship)

• Deprived of liberty Subject (by judicial or administrative decision)

Related Conditions & MeSH terms

• Movement Disorders
• Pronation-Supination of the Forearm, Impairment of

Intervention

Diagnostic Test:
• 4D-CT-scan
Both forearms of the subjects with posttraumatic forearm impairment are scanned with a 4D-CT scanning technique, during forearm rotation.

Locations

Country	Name	City	State
France	CHU Montpellier	Montpellier

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quantification of forearm motion patterns	Calculate the mean and standard deviation of the healthy versus the affected forearm rotation.	the 4D-CT-scan procedure