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

NCT ID: NCT04067232

Last Updated: 2022-12-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 5 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-01-16
• Study Completion Date: 2020-06-15

Brief 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.

Detailed 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.

Conditions

Pronation-Supination of the Forearm, Impairment of

Keywords

Four Dimensional Computed Tomography (4D-CT)

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Patients with posttraumatic forearm impairment

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

Group Type: EXPERIMENTAL

4D-CT-scan

Intervention Type: DIAGNOSTIC_TEST

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

Interventions

4D-CT-scan

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

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

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 (βHCG 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)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Montpellier

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Geert BUIJZE, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Montpellier

Locations

CHU Montpellier

Montpellier, , France

Countries

France

Other Identifiers

UF 7729

Identifier Type: OTHER

Identifier Source: secondary_id

RECHMPL18_0463

Identifier Type: -

Identifier Source: org_study_id