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Assessment of Nutritional Status in Systemic Sclerosis

Assessment of Nutritional Status in Systemic Sclerosis: Prospective Cohort Study in Montpellier University Hospital

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04301596
Acronym
NUTRISCLER
Enrollment
150
Registered
2020-03-10
Start date
2020-06-12
Completion date
2024-10-12
Last updated
2023-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Systemic Sclerosis

Brief summary

The main theme of the cohort of systemic sclerosis (SSc) patients is the determination of nutritional status, its evolution and the evaluation of its management in patients with scleroderma. The main objectives are : * To determine the incidence of malnutrition and its main determinants (disease characteristics, severity, eating habits, physical activity) in patients with scleroderma. * For patients with undernutrition at inclusion or at 18 months follow-up: evaluate the impact of a standardized nutritional intervention (dietary advice, oral supplements, artificial, enteral or parenteral nutrition) on nutritional and disease parameters. Follow-up visits will take place every 6 months for 2 years. (M6, M12, M18 et M24). During each visit: a clinical examination, with anthropometric measurements, a 3-day dietary survey and a blood sample (10 ml), completion a multiple-choice of quality of life and physical activity evaluation. Paraclinical evaluation : echocardiography, lung function tests, screening for osteoporosis (M6 and M18). If undernutrition is detected during a follow-up visit, the subject will be referred to a specialized service.

Interventions

different set of data will be collected over a 6 months period

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All SSc patients aged 18 or more * Patient followed at the Montpellier University Hospital * Patients must fulfil the American College of Rheumatology (ACR) and European League Against Rheumatism (EULAR) 2013 criteria for SSc. * Health insurance (affiliation to social security) * Collection of non-opposition to participate in the study

Exclusion criteria

* Patient under the protection of justice curatorship / guardianship; * Patients who have already planned to move out of the region in the next two years, making the follow-up impossible.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of malnutrition6 monthsIncidence of malnutrition will be measured as a loss of more than 10% of body weight or a body mass index (BMI) less than 21 kg/m2
Idetification of risk factors associated with malnutrition6 monthsCollection of data related to SSc disease burden
Success of the nutritional intervention6 monthsbody weight gain \> 5%

Countries

France

Contacts

Primary ContactAlexandre MARIA, MD, PhD
a-maria@chu-montpellier.fr+33467337332
Backup ContactPhilippe GUILPAIN
p-guilpain@chu-montpellier.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026