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Clinical Trials/NCT04791280
NCT04791280
Unknown
Not Applicable

Study of the Intestinal Microbiota of Patients With Systemic Sclerosis

Assistance Publique - Hôpitaux de Paris1 site in 1 country200 target enrollmentMarch 31, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Systemic Sclerosis
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
200
Locations
1
Primary Endpoint
Prevalence of dysbiosis
Last Updated
3 years ago

Overview

Brief Summary

The term gut microbiota describes the entire intestinal microbial communities. Studies have established the important role played by the gut microbiome in modulating vital functions of the healthy host. The physiological effects of the microbiota for the host are, for the most part, beneficial. In several pathologies, an imbalance in the composition of the microbiota has been demonstrated.

Systemic sclerosis is an autoimmune, disorder of the connective tissue, characterized by vascular lesions, immunological abnormalities, and fibrosis of skin and internal organs As in many inflammatory diseases, there are painful digestive manifestations in systemic scleroderma that affect up to 90% of patients. The exact pathophysiology of the digestive involvement in systemic sclerosis is uncertain. The digestive manifestations of systemic sclerosis are frequent and can affect the entire digestive system.

However, there are few studies of the intestinal microbiota in this disease, which seems to be part of the same continuum of diseases with abnormalities of innate immunity. By analogy with chronic inflammatory bowel diseases, particularly Crohn's disease, we have raised the question of the existence of dysbiosis during scleroderma which could lead to episodes of acute, severe and recurrent inflammation of the peritoneum under the influence of triggering factors. The long-term prospects would be to look for ways to prevent attacks or to treat them more rapidly and effectively by using therapeutic targets in the intestinal microbiota.

The study population will be seen in the usual care setting, identically to all patients with systemic sclerosis treated in the department.

In case of an inflammatory disease outbreak, and depending on its severity, the patient will be seen again in consultation or hospitalized. Appropriate complementary examinations (biology, imaging, endoscopy) will be carried out and the treatment adapted.

Registry
clinicaltrials.gov
Start Date
March 31, 2021
End Date
September 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years old
  • Patient with a confirmed diagnosis of systemic sclerosis according to international criteria, before or after the start date of this study.
  • Non-opposition of the patient

Exclusion Criteria

  • Subject under guardianship, curatorship or safeguard of justice
  • Subject with state medical aid (AME)
  • Subject does not speak French
  • Subject unable to answer questions or express himself/herself
  • Taking antibiotics or a colonic preparation within 6 weeks prior to stool collection will be a temporary contraindication to stool collection. The patient may be included, other usual care samples may be taken, but the stool sample will be deferred and taken at a later date.

Outcomes

Primary Outcomes

Prevalence of dysbiosis

Time Frame: Throughout the whole study, up to 6 months

to study the prevalence of dysbiosis in patients with systemic sclerosis treated in the internal medicine department of St. Antoine Hospital in order to investigate prognostic biological parameters of disease progression, response to treatment and the occurrence of intestinal and extra-intestinal complications.

Secondary Outcomes

  • The fecal bacterial composition in comparison to different subtypes of systemic sclerosis and evolution during the time(Throughout the whole study, up to 6 months)
  • Microbiota correlation(Throughout the whole study, up to 6 months)
  • Microbiota composition and diversity assessed by 16s sequencing(Throughout the whole study, up to 6 months)

Study Sites (1)

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