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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03350685
Other study ID # WHO (29BRC17.0179)
Secondary ID
Status Completed
Phase N/A
First received November 17, 2017
Last updated February 12, 2018
Start date November 15, 2017
Est. completion date February 9, 2018

Study information

Verified date February 2018
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Whipple's disease is a chronic systemic infection caused by ubiquitous bacterium Tropheryma wipplei on a genetic predisposition which should be considered in patients with recurrent episodes of seronegative arthritis, erosive or not, or inflammatory low back pain, chronic diarrhea, persistent fever, unexplained neurological signs, uveitis, endocarditis, and epithelioid granuloma.

Laboratory tests may show malabsorption, erythrocyte sedimentation rate and C-reactive protein elevation, anemia, thrombocytosis, eosinophilia and lymphopenia.

None of theses findings is specific and most patients have arthritis or low back pain mimicking rheumatoid arthritis and spondyloarthritis.

As the disease is rare, chance for positive polymerase chain reaction testing for Tropheryma whipplei is low in this context.


Recruitment information / eligibility

Status Completed
Enrollment 267
Est. completion date February 9, 2018
Est. primary completion date February 9, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult

- patient with at least a screening test for Whipple'disease

- participation agreement,

Exclusion Criteria:

- No test for Whipple'disease

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France CHU d'ANGERS Angers
France CHRU de Brest Brest
France CH le MAns Le Mans
France CHU de Nantes Nantes
France CH d'ORLEANS Orleans
France CHU de POITIERS Poitiers
France CHU de Rennes Rennes
France CHU de Tours Tours

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients diagnosed as whipple's disease Diagnosis of Whipple's disease based on
at least one suggestive clinical finding
at least one test detecting T. Whipplei
diagnosis made by a specialist
a dramatic and persistent response to antibiotic therapy
Hydroxychloroquine 200mgx2 plus Doxycycline 100mgx2
or trimethoprim/sulfamethoxazole 800/160mg x2
Day 0 ( Date of diagnostic)
Secondary Number of test performed in each centre Number of diagnoses according to tests
Patients will be divided into three groups
Classic Whipple's disease (CWD), defined as :
duodenal biopsy positive by PAS/immunohistochemistry
or blood positive by PCR
Focal Whipple's disease (FWD)
joint fluid positive by PCR
but duodenal biopsy negative by PAS/immunohistochemistry
Chronic T. whipplei-associated arthritis (CTWA): chronic arthritis and
duodenal biopsy, stool, or saliva positive by PCR
duodenal biopsy negative by PAS/immunohistochemistry
joint fluid negative by PCR
Day 0 (Date of diagnostic)