- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04297475
The Clinical Feasibilityof a Multi-modal Photoacoustic/Ultrasonic Imaging System in Rheumatoid Arthritis
October 26, 2020 updated by: Peking Union Medical College Hospital
The Clinical Feasibility and Added Value of a Multi-modal Photoacoustic/Ultrasonic Imaging System in the Evaluation of Rheumatoid Arthritis
New type of imaging method is in demand clinically for early detection and treatment guiding of RA.
Photoacoustic imaging (PAI), a hot spot in medical imaging society, which combines the merits of optical imaging and US and has a capacity in morphological, functional and molecular imaging, has shown potential in visualizing superficial organs, including small joints.
The investigators developed a multi-modal photoacoustic/ultrasound (PA/US) imaging system, equipped with a handheld 3D PA/US probe, which wass able to provide 3D volume data of dual-wavelength PA imaging of small joints, in addition to real-time 2D PA/US imaging.
The investigators plan to recruit RA patients in different disease conditions and healthy volunteers to receive the 2D and 3D PA/US examination on the 2nd and 3rd MCP, PIP joints and wrist joints using this imaging system, and to evaluate the potential clinical role of the imaging system in RA, and its added value to current imaging methods.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
The multi-modal PA/US imaging system was built on a high-end commercial US platform, and allowed real-time imaging of grey-scale US imaging, Color-Doppler US (CDUS) imaging and dual-wavelength PA imaging.
The PA/US images were acquired using a hand-held probe integrated optical devices and US transducers.
3D volume data of the selected joint of each participant was collected using an automatic scanning device after the dual-modal imaging.
The investigators plan to recruit RA patients from the outpatient department of Rheumatology of our hospital, who have been diagnosed as RA by experienced rheumatologists.
The patients and healthy volunteers will receive multi-modal imaging examinations using the novel imaging system.
The MCP 2 and 3, PIP 2 and 3, and wrist of bilateral hand were chosen for the multi-modal imaging.
Conventional US scanning of the joints, including grey-scale US, CDUS, and PDUS, will be carried out by an experienced US operator.
Afterwards, 2D and 3D PA/US imaging will be implemented for each joint by the same operator.
All of the imaging data will be analysed by the Matlab software.
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Beijing
-
Beijing, Beijing, China, 100730
- Recruiting
- Peking Union Medical College Hospital
-
Principal Investigator:
- Meng Yang, Doctor
-
Sub-Investigator:
- Chenyang Zhao, Doctor
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The RA patients are diagnosed as RA by two experienced rheumatologists.
Description
The inclusion criteria
- The patients were above 18 years-old;
- The patients were diagnosed with RA according to the American College of Rheumatology (ACR) criteria, and the current clinical state was in-active or relapse;
- The patients were consent to receive examinations of photoacoustic imaging.
The exclusion criteria
- The patients had mental disease or other severe diseases, and were not capable of receiving imaging examinations;
- The patients had strong reaction to laser light.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
rheumatoid arthritis
The patients are diagnosed with RA according to the American College of Rheumatology (ACR) criteria, and the current clinical state was in-active or relapse.
The patients receive final diagnosis and disease evaluation by two experienced rheumatologists
|
The multi-modal PA/US imaging system is equipped with a handheld 3D PA/US probe, and able to provide 3D volume data of dual-wavelength PA imaging of small joints, in addition to real-time 2D PA/US imaging.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The PA scores of 50 participants with RA identified by the multi-modal imaging system are in accordance with clinical scoring
Time Frame: 3-6 months
|
A total of 50 participants received semi-quantitatively measurement of PA signals by the imaging system using a 0-3 scoring system.
Score 0 is no PA signals, which represents no detectable active inflammation on PA imaging.
Score 1 means less than 3 bars of PA signals within the inflamed regions.
Score 2 means multiple PA signals within less than half of the inflammatory lesions.
And score 3 means abundant PA signals in over half of the lesions of RA synovium or tenosynovium, which may represent high inflammation activity.
|
3-6 months
|
|
The functional imaging of 60 RA patients assessed by the multi-modal imaging system
Time Frame: 12-15 months
|
The oxgenation levels of local joint tissues of 60 RA patients are measured by dual-wavelength PA imaging.
|
12-15 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Yuxin Jiang, Doctor, Peking Union Medical College Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
January 1, 2019
Primary Completion (ANTICIPATED)
December 31, 2021
Study Completion (ANTICIPATED)
December 31, 2022
Study Registration Dates
First Submitted
July 13, 2019
First Submitted That Met QC Criteria
March 3, 2020
First Posted (ACTUAL)
March 5, 2020
Study Record Updates
Last Update Posted (ACTUAL)
October 28, 2020
Last Update Submitted That Met QC Criteria
October 26, 2020
Last Verified
September 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MMPAUS RA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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