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Sensitivity of Echography in Arthritis (SEA)

Primary Purpose

Rheumatoid Arthritis

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
ultra-sonography
Sponsored by
Association de Recherche Clinique en Rhumatologie
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Rheumatoid Arthritis focused on measuring synovitis score, sensitivity to change, clinical examination, ultra-sonography

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with rheumatoid arthritis meeting ACR criteria.
  • Justifying anti-TNF alpha treatment (switch or first administration).
  • To have at least 6 synovitis at the clinical examination necessary for the DAS evaluation
  • To accept to participate in this study (informed consent signed).

Exclusion Criteria:

  • Minor patients.
  • Pregnancy.
  • Breastfeeding.

Sites / Locations

  • CHU-Brugmann
  • Hôpital Ambroise Paré
  • CHU de la Cavale Blanche
  • CHU Côte de Nacre
  • CHU A. Michallon
  • Hôpital Bicêtre
  • Hôpital Cochin
  • Hôpital de la Pitié
  • CHU de RENNES - Hôpital Sud
  • CHU Nancy-Brabois

Outcomes

Primary Outcome Measures

joint score evaluated by clinical examination
joint score evaluated by ultra-sonography

Secondary Outcome Measures

DAS28 Synovial index
ACR Synovial index (66 sites)

Full Information

First Posted
March 7, 2007
Last Updated
August 25, 2009
Sponsor
Association de Recherche Clinique en Rhumatologie
Collaborators
RCTs
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1. Study Identification

Unique Protocol Identification Number
NCT00444691
Brief Title
Sensitivity of Echography in Arthritis
Acronym
SEA
Official Title
Sensitivity of Echography in Arthritis
Study Type
Interventional

2. Study Status

Record Verification Date
August 2009
Overall Recruitment Status
Unknown status
Study Start Date
March 2007 (undefined)
Primary Completion Date
August 2008 (Actual)
Study Completion Date
April 2010 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Association de Recherche Clinique en Rhumatologie
Collaborators
RCTs

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
It has been reported recently that the detection of synovitis by ultrasonography was more sensitive than clinical examination (Wakefield et al. Ann Rheum Dis). An OMERACT and EULAR working party recently produced guidelines on the best way to record and score quantitatively synovitis of the small joints of the hands and feet (Wakefield R, D'Agostino MA). It has also been presumed recently that ultrasonography was more sensitive to changes than clinical examination after anti-TNF treatment (Ref. Taylor et al). If this better sensitivity to change were to be confirmed, ultrasonography would be preferred to clinical examination in studies evaluating new treatments. In everyday practice, better intrinsic validity of the evaluation of synovitis by ultrasonography would lead to widespread use of this technique in the diagnosis and treatment of rheumatoid arthritis patients. Objective of this study is to compare the sensitivity to change in synovitis score according to the monitoring method used (clinical examination versus ultrasonography).
Detailed Description
This is a multicenter, (10 French centers and 1 Belgian center), prospective (4-month patients' follow-up) interventional study in 120 patients with rheumatoid arthritis justifying anti-TNF treatment. The overall duration of the study will be 8 months composed of a 4-month inclusion period and a 4-month follow-up period for each patient. Moreover, X-ray evaluations of hands and feet will be performed 2 years from the beginning of the study in order to assess the changes in structural damage. During the patients' participation, 6 visits are planned: an inclusion visit then, a follow-up visit at 1, 2 and 3 months from the inclusion visit, and a final evaluation visit at 4 months from the inclusion visit. At each visit, synovitis will be evaluated using both methods: clinical examination and ultrasonography. For a same patient, clinical evaluation of synovitis will have to be performed - during the entire study - by the same rheumatologist and the ultrasonographic evaluation will have to be performed by the same ultrasonographist (different from the rheumatologist) and always using the same ultrasonograph. Finally, patients will be performed anterior X-rays of hands and feet two years from the beginning of the study whatever the ongoing RA treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rheumatoid Arthritis
Keywords
synovitis score, sensitivity to change, clinical examination, ultra-sonography

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
ultra-sonography
Other Intervention Name(s)
scanners:, ESAOTE Technos MPX, TOSHIBA APLIO, ESAOTE MyLab, PHILIPS HD11, BK Mini Focus.
Intervention Description
o The ultrasonographic evaluation was performed on 38 joints: the 28 joints included in DAS28 (e.g. shoulderx2, elbowx2, wristx2, metacarpo-phalangeal (MCP)x10, proximal inter phalangeal (PIP)x10, kneex2) and also the metatarso-phalangeal (MTPx10). Systematic multiplanar gray-scale (mode B) and Power Doppler examination was carried out with commercially available real-time scanners using multi-frequency linear transducers (7-12 MHz). The ultrasonographic evaluation was performed at baseline and 1, 2, 3, and 4 months after baseline.
Primary Outcome Measure Information:
Title
joint score evaluated by clinical examination
Time Frame
baseline and 1, 2, 3 and 4 months after baseline
Title
joint score evaluated by ultra-sonography
Time Frame
baseline and 1, 2, 3 and 4 months after baseline
Secondary Outcome Measure Information:
Title
DAS28 Synovial index
Time Frame
baseline and 1, 2, 3 and 4 months after baseline
Title
ACR Synovial index (66 sites)
Time Frame
baseline and 1, 2, 3 and 4 months after baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with rheumatoid arthritis meeting ACR criteria. Justifying anti-TNF alpha treatment (switch or first administration). To have at least 6 synovitis at the clinical examination necessary for the DAS evaluation To accept to participate in this study (informed consent signed). Exclusion Criteria: Minor patients. Pregnancy. Breastfeeding.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maxime DOUGADOS, Professor
Organizational Affiliation
ARCR
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU-Brugmann
City
Bruxelles
ZIP/Postal Code
1020
Country
Belgium
Facility Name
Hôpital Ambroise Paré
City
Boulogne
ZIP/Postal Code
92104
Country
France
Facility Name
CHU de la Cavale Blanche
City
Brest
ZIP/Postal Code
29609
Country
France
Facility Name
CHU Côte de Nacre
City
Caen
ZIP/Postal Code
14000
Country
France
Facility Name
CHU A. Michallon
City
Grenoble
ZIP/Postal Code
38000
Country
France
Facility Name
Hôpital Bicêtre
City
Le Kremlin Bicetre
ZIP/Postal Code
94275
Country
France
Facility Name
Hôpital Cochin
City
Paris
ZIP/Postal Code
75006
Country
France
Facility Name
Hôpital de la Pitié
City
Paris
ZIP/Postal Code
75013
Country
France
Facility Name
CHU de RENNES - Hôpital Sud
City
Rennes
ZIP/Postal Code
35000
Country
France
Facility Name
CHU Nancy-Brabois
City
Vandoeuvre Les Nancy
ZIP/Postal Code
54511
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
27042336
Citation
Cheung PP, Mari K, Devauchelle-Pensec V, Jousse-Joulin S, D'Agostino MA, Chales G, Gaudin P, Mariette X, Saraux A, Dougados M. Predictive value of tender joints compared to synovitis for structural damage in rheumatoid arthritis. RMD Open. 2016 Mar 17;2(1):e000205. doi: 10.1136/rmdopen-2015-000205. eCollection 2016.
Results Reference
derived

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Sensitivity of Echography in Arthritis

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