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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04499040
Other study ID # 2016-42
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2020
Est. completion date December 31, 2023

Study information

Verified date July 2020
Source Assistance Publique Hopitaux De Marseille
Contact Alexandre FABRE
Phone 491382747
Email alexandre.fabre@ap-hm.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objectives: Collect clinical and biological data about patients with SD/THE, collect samples of patients; create a secure on line database to collect worldwide data about SD/THE Partners : APHM, HCL, APHP

Currently10 patients (8 with TTC37 mutations and 2 with SKIV2l mutations) present a SD/THE and are managed in France in 5 different centers (Marseille, Paris Trousseau, Paris Necker, Paris Robert Debrés, and Lyon). Most of them are followed in hepato-gastro-enterology units for their intractable diarrhea. Three aspects of the disease: intractable diarrhea, immune defect and liver disease are responsible for the main part of the burden of the disease .For each aspect, the investigators will propose a close follow-up with collection of clinical, biochemical, functional and microbial data.

Collect of clinical date: during a programmed consultation clinical data about symptom will be collected twice a year. A detailed form will be used for better delineation of the symptoms. These data included growth, symptom (diarrhea, pain …), and clinical signs. Most of these children have recurrent sample for follow up. During them some blood will be take for study the immune side but also the platelet function.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 31, 2023
Est. primary completion date August 31, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- patient < 18 year-old

- patients with SD/THE

control group :

- patients with tufting enteropathy and short bowel syndrome.

Exclusion Criteria:

- child among whom the parents or the legal representatives refused that their child participates in this study

Study Design


Intervention

Biological:
Blood sample
Blood samples to assess biological parameters such as:
Other:
Fecal samples
Microbiota analysis
Behavioral:
Neuropsychological
Neuropsychological assessment

Locations

Country Name City State
France Assistance Publique Hopitaux de Marseille Marseille

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of detailed clinical characteristics of the phenotype of Tricho-hepato-enteric syndrome Existence or absence of 9 clinical signs suggestive of Tricho-hepato-enteric syndrome, to know:
neonatal characteristics,
existence or not of the 9 clinical signs suggestive of the disease,
initial symptoms and chronology leading to the diagnosis,
organ damage,
nutrition,
treatment,
growth,
dermatological evaluation,
hepatic evaluation,
neuropsychological evaluation (score of WPPSI-III, WISC-IV, WAIS-IV),
quality of life scale (VSPA in children between 3 and 17 years old and WHOQUOL in adults),
self-report anxiety scale (STAI in children over 8 years)
3 years