ECHORTON: Validation of a Diagnostic Algorithm of Giant Cell Arteritis

Sponsor
Poitiers University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02703922
Collaborator
Groupe Hospitalier de la Rochelle Ré Aunis (Other), Centre Hospitalier de Rochefort (Other)
168
6
1
65.4
28
0.4

Study Details

Study Description

Brief Summary

Giant cell arteritis (GCA or temporal arteritis or cranial arteritis) or Horton disease is a vasculitis that occurs in older adults, affecting vessels of medium and large caliber. The diagnosis of GCA is a challenge for general practitioners and specialists. Since 1970, it is based on a combination of clinical, biological and histological signs. Temporal artery biopsy (TAB) was the reference method until recently. However, TAB has many drawbacks. Therefore, researches of the past 20 years have been intended to develop alternative diagnostic methods. This was notably the case of the color Doppler ultrasound (CDU) since the description by Wolfgang Schmidt of the halo sign. Although European and British recommendations put CDU as second line method, many authors suggest the possibility to do without TAB in many cases. In addition, many practitioners believe that it is not "ethical" to use an invasive unprofitable procedure like TAB, and have already been using CDU in their routine practice. However, no diagnostic algorithm validating this approach in a prospective series has been published to date. Therefore, the present study aim at validating a diagnostic algorithm of giant cell arteritis using color Doppler imaging of temporal arteries and cervicocephalic axes as first screening method.

Condition or Disease Intervention/Treatment Phase
  • Other: color Doppler ultrasound and TAB in case of CDU negative
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
168 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Validation d'un Algorithme Diagnostique de l'artérite Temporale Giganto-cellulaire basé Sur l'échographie-doppler Couleur Des artères Temporales Superficielles et Des Axes Cervico-encéphaliques
Actual Study Start Date :
Aug 29, 2016
Actual Primary Completion Date :
Feb 10, 2020
Actual Study Completion Date :
Feb 10, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: GCA suspicion

A first screening is performed using color Doppler ultrasound. In case of negative results, patients undergo TAB.

Other: color Doppler ultrasound and TAB in case of CDU negative
Screening with color Doppler ultrasound followed by TAB in case of CDU negative

Outcome Measures

Primary Outcome Measures

  1. Number of CDU false-positive patients [after 2 years of follow-up]

    patients with an alternative diagnosis within 2 years of follow-up among patients considered with GCA on a clinico-biological suspicion + Doppler "positive."

Secondary Outcome Measures

  1. rate of "TAB positive" among "negative or doubtful CDU " [within 1 month (during diagnostic algorithm)]

    Number of TAB positive patients per patients with negative or doubtful CDU

  2. Number of patients with a persistent Halo at second CDU examination [after 2 years of follow-up]

    Describe S3/S4 Halo changes, and study correlation between persistence and poorer clinical response

  3. Number of correctly interpreted TAB [1 month (after second blind reading of histological specimen and doppler imaging)]

    Reproducibility of TAB interpretation

  4. Number of correctly interpreted CDU [1 month (after second blind reading of histological specimen and doppler imaging)]

    Reproducibility of CDU interpretation

  5. Cost-result of the algorithm [after 2 years of follow-up]

    Diagnostic costs, induced costs, avoided costs

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • ≥ 50 years

  • C reactive protein (CRP) above normal

  • Suspected of GCA according to clinician expertise and / or aortitis arteritis or of one or more arteries from the aorta imaging (CT angiography, magnetic resonance angiography or positron emission tomography TDM18FDG)

  • Benefiting from Social Security or receiving it via a third party

  • have given their participation agreement by understanding and accepting the constraints of the study

Exclusion Criteria:
  • Received corticosteroid dose ≥ 20 mg of prednisone equivalent for more than 7 days in the month before inclusion

  • Underwent temporal artery biopsy before color Doppler ultrasound

  • History of GCA

  • Terminal palliative phase or suffering from a disease or comorbidities such as life is involved in less than a year

  • Patient with severe cognitive impairment

  • Patient that can not be followed by the investigator for the duration of the study

  • Refusal to participate in the study

  • With enhanced protection (namely those deprived of liberty by a court or administrative order, patient staying in a health or social institution, under legal protection, and patients in emergencies)

  • Pregnant or breastfeeding women, women of childbearing age who do not have effective contraception

  • Participating in another clinical trial.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier d'Angoulême Angoulême France
2 Groupe Hospitalier de la Rochelle Ré Aunis La Rochelle France 17019
3 Centre Hospitalier Universitaire de Nantes Nantes France
4 Centre Hospitalier de Niort Niort France 79021
5 Centre Hospitalier Universitaire de Poitiers Poitiers France 86021
6 Centre Hospitalier de Rochefort Rochefort France 17301

Sponsors and Collaborators

  • Poitiers University Hospital
  • Groupe Hospitalier de la Rochelle Ré Aunis
  • Centre Hospitalier de Rochefort

Investigators

  • Study Director: Christophe Roncato, MD, Groupe Hospitalier de la Rochelle Ré Aunis
  • Study Director: Guillaume Denis, MD, Centre Hospitalier de Rochefort

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Poitiers University Hospital
ClinicalTrials.gov Identifier:
NCT02703922
Other Study ID Numbers:
  • ECHORTON
First Posted:
Mar 9, 2016
Last Update Posted:
Apr 20, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 20, 2022