4DCT Wrist Reference and DRUJ

NCT ID: NCT05886426

Last Updated: 2023-06-02

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 60 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-08-01
• Study Completion Date: 2024-02-01

Brief Summary

The study will consist of 3 parts. First a reference study is performed with healthy volunteers to investigate the viability of 4DCT scanning of the wrist for evaluating wrist bones configurations and movements (translations and rotations) during a new set of wrist motions that have not been evaluated in our previous study focused on the scapholunate ligament (NL72518.091.19). The following will be evaluated: the visibility of the DRUJ, the carpal metacarpal 1 (CMC-1) joint and the metacarpal phalangeal 1 (MCP-1) joint during clinically relevant wrist movements. Besides, in this study the difference is evaluated between between the left right wrist within participants during wrist motion. In future clinical practice the uninjured wrist may be used as a reference for the injured wrist, determining the left right difference in healthy volunteers will show the robustness of this technique. Subsequently a reliability study is performed to investigate the intra-patient test-retest reliability of our 4DCT scanning protocol. Lastly a diagnostic clinical study is performed on patients with chronic wrist pain, suspect for DRUJ instability. The objective of the clinical study is to determine the sensitivity and specificity of the 4DCT scan (during a series of movements in which DRUJ instability is predicted to be best visible) in the diagnosis of DRUJ instability in comparison with arthroscopic findings (gold standard). If the 4DCT shows to have a sensitivity and specificity comparable to that of wrist arthroscop

Detailed Description

Single institution, a explorative volunteer study with participants followed by a prospective clinical study in the Radboud University Medical Center.

30 healthy participants will be included who have no medical history of wrist trauma, surgery or wrist complaints and in age range of 20-50 and; and 30 patients with chronic unilateral wrist pain suspect for DRUJ instability.

For the volunteer study all 30 healthy participants first undergo a bilateral 3D CT scan in neutral wrist position for usage of reference. The field of view of this scan includes all carpal bones and the two forearm bones. The scan technique is a Toshiba delivered application and CE certified. Subsequently, the forearms are placed in a supporting frame which minimizes lower-arm motion during 4DCT image acquisition. Prior to image acquisition, participants will undergo a training session on how to move their wrist according to the imaging protocol. A bilateral dynamic 4DCT scan is made while actively moving the wrists according to a protocoled cycle of movements. To reduce radiation exposure, the z-axis coverage is reduced to 12 cm in the 4DCT scan. Videos of the wrist movements are shown to the participant during image acquisition, which will help the participants to perform the movements at a constant pace. This will provide images with highest quality and will provide the source data considering carpal bone movements and function of ligaments during active wrist motions.

For the reliability study 20 of the participants included in the volunteer study will additively undergo an extra unilateral 4DCT scan at least 15 minutes after the bilateral 4DCT scan. Which wrist is scanned is decided by random selection. Except for the scanning being performed unilateral instead of bilateral the protocol is exactly the same as the 4DCT protocol as described above.

For this DRUJ instability study, a static 3D CT scan and a dynamic 4DCT scan of the both wrists of the patient suspect for DRUJ instability will be done after the X ray which is performed during standard clinical practice. The protocol is the same as described above in the volunteer study but the patients follow the DRUJ movement protocol with movements that are clinically relevant for DRUJ instability diagnosis.

The following radiographic signs will be evaluated: radioulnar angle; sigmoid notch to ulnar head joint distance; radioulnar ratio; radioulnar line distance; subluxation ratio; epicentre distance; radioulnar joint volume; ulnar variance and ulnar head to carpal bones joint distance [25] [26] [27] [30] [31].

Conditions

Distal Radioulnar Joint Sprain

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Reference study

Healthy participants (bilateral scans so 60 wrists) will be needed for the volunteer study to determine the visibility of the wrist joints (DRUJ, CMC-1 and MCP-1); acquire normal values and investigate the left right differences between the wrists

4DCT wrist and standard CT wrist

Intervention Type: DIAGNOSTIC_TEST

Dynamic CT aquistion of wrist during movement and standard static wrist CT

Reliability study

Healthy participants (20 wrists) that underwent a 4DCT scan for the volunteer study will be needed to undergo a second unilateral scan to investigate the intra-patient test-retest reliability of the protocol

4DCT wrist and standard CT wrist

Intervention Type: DIAGNOSTIC_TEST

Dynamic CT aquistion of wrist during movement and standard static wrist CT

DRUJ instability group

Patients with chronic unilateral wrist pain, in this study suspect for DRUJ instability, will be studied to evaluate the effect of TFCC injury on the wrist kinematics and evaluate the use of 4DCT for the diagnosis of TFCC injury

4DCT wrist and standard CT wrist

Intervention Type: DIAGNOSTIC_TEST

Dynamic CT aquistion of wrist during movement and standard static wrist CT

Interventions

4DCT wrist and standard CT wrist

Dynamic CT aquistion of wrist during movement and standard static wrist CT

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• Between 18-50 years (healthy volunteer only)
• A 3D CT scan is required.
• Informed consent from both the healthy volunteer and patient.

Exclusion Criteria

A participant who meets any of the following criteria will be excluded from participation in the volunteer study:

• < 18 year and > 50 years
• medical history of wrist: trauma, pain and/or surgery
• persons with limited wrist movements
• wrists with arthritis on plain radiograph or 3D CT scan
• pregnancy

A patient with suspicion of DRUJ instability who meets any of the following criteria will be excluded from participation in the clinical study:

• medical history of wrist fracture, known ligament lesion other than the TFCC and/or wrist surgery
• inability to undergo diagnostic arthroscopy
• wrists with arthritis on plain radiograph or 3D CT scan
• pregnancy

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Radboud University Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Brigitte van der Heijden, Dr.

Role: PRINCIPAL_INVESTIGATOR

Radboud University Medical Center

Central Contacts

Brigitte van der Heijden, Dr.

Role: CONTACT

Brigitte.vanderheijden@radboudumc.nl

+31644009575

Other Identifiers

114440

Identifier Type: -

Identifier Source: org_study_id