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Registry for Patients With Lipodystrophy

Recruiting
Conditions
Lipodystrophy Acquired
Lipodystrophy Congenital
Registration Number
NCT03553420
Lead Sponsor
University of Ulm
Brief Summary

Given the lack of knowledge on lipodystrophies, the medical and social responsibility for the persons affected by it calls for the monitoring of the progression over long periods of time. Sensible clinical and basic research into rare diseases such as lipodystrophy is only possible in multi-location networks with sufficient case numbers. Also, reliable information on the incidence of certain manifestation patterns, health status, etc. is of utmost importance for health care and health policy in this rare disease.

Therefore, the European Consortium of Lipodystrophies (ECLip), an association of European experts on lipodystrophy, has launched a registry (OSSE) for lipodystrophies which is committed to help to improve the research conditions by consolidating this kind of information in a registry.

Detailed Description

As lipodystrophies are rare diseases subdivided into yet rarer sub-groups, research in this field requires international co-operation.

The European Consortium of Lipodystrophy (ECLip) consists of an association of European experts in the field of lipodystrophy. It has set up a Registry Board to implement a registry for patients with lipodystrophy using the Open Source Software OSSE (Open Source Registry System for Rare Diseases in the EU), which is a web based platform focused on a federated approach that allows to perform distributed searches which are designed to comply data protection requirements and preserve data sovereignty. To ensure data protection, medical and identifying data will be stored on two different servers both run by the Institute for Epidemiology and Medical Biometry of the University of Ulm.

Medical centers from all over the world where patients are treated with lipodystrophy are invited to join the ECLip Registry and to become ECLip Registry members. Upon registration, they can enter patient data after they have obtained local ethic committee permission and the patient in question has given written consent to this. Data entry is done at the individual locations via a web-based user interface. Identifying data are recorded directly into the identity management system. Communication between the identity management and the OSSE registry happens via a web browser.

The aim of the patient registry is to compile data on the natural history of each different sub-group of lipodystrophies, their comorbidities, treatment options used and medical and quality of life out-come for the patients. For this, the following data retrieved from regular patient visits are collected:

* Precise diagnosis including moleculargenetic results

* Clinical presentation and comorbidities

* Laboratory changes and results of diagnostic procedures

* Natural course of the disease including age at onset of disease and comorbidities

* Family history

Research within this registry can be performed by participating clinicians/researchers and third parties after a research proposal has be accepted by the responsible committee of the ECLip. The registry aims to answer the following questions

* new insights into the pathophysiology of lipodystrophy

* improve therapeutic options for the patients

* compile information material for patients, families and relevant professionals

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
5000
Inclusion Criteria
  • lipodystrophy
Exclusion Criteria
  • lipodystrophy due to anti-retroviral drugs

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Age at deathafter 20 years

patients are followed regularly, age at death (years) will be documented

Secondary Outcome Measures
NameTimeMethod
change in somatic comorbidities under standard treatmentyearly for 50 years

standardized physical examination, laboratory and instrument based tests

age at onset of metabolic complicationsyearly for 50 years

metabolic complications will be assessed via standardized physical examination, laboratory and instrument based tests

age at onset orthopedic complicationsyearly for 50 years

orthopedic complications will be assessed via standardized physical examination, laboratory and instrument based tests

genotype-phenotype correlation for patients with familial lipodystrophyevery 5 years for 50 years

molecular genetic results will be compared to results from standardized physical examination, laboratory and instrument based tests

age at onset neuromuscular complicationsyearly for 50 years

neuromuscular complications will be assessed via standardized physical examination, laboratory and instrument based tests

Trial Locations

Locations (19)

Med. Klinik B für Gastroenterologie und Hepatologie, Universitätsklinikum Münster

🇩🇪

Münster, Germany

Santiago de Compostela University

🇪🇸

Santiago de Compostela, Spain

Endocrinology Unit, Department of Clinical and Medical science, S. Orsola-Malpighi Hospital , University of Bologna

🇮🇹

Bologna, Italy

Academic Medical Center, University of Amsterdam

🇳🇱

Amsterdam, Netherlands

Ostschweizer Kinderspital

🇨🇭

Saint Gallen, Switzerland

Medical University of Vienna

🇦🇹

Vienna, Austria

University of Szeged, Department of Internal Medicine

🇭🇺

Budapest, Hungary

Lille University

🇫🇷

Lille, France

Pierre et Marie Curie School of Medicine, Sorbonne University

🇫🇷

Paris, France

Department of Internal Medicine (Endocrinology and Nephrology), University of Leipzig

🇩🇪

Leipzig, Germany

Dept for Pediatrics and Adolescent Medicine, University of Ulm: Interdisciplinary obesity clinic

🇩🇪

Ulm, Germany

Tor Vergata University - Policlinico of Tor Vergata

🇮🇹

Roma, Italy

Universita del piemonte Orientale

🇮🇹

Novara, Italy

Endocrine Unit of University Hospital of Pisa

🇮🇹

Pisa, Italy

University of Cambridge Metabolic Research Laboratories

🇬🇧

Cambridge, United Kingdom

Abel Salazar Biomedical Sciences Institute - University of Porto

🇵🇹

Porto, Portugal

University Medical Center Ljubljana - Clinical Institute of Medical Genetics

🇸🇮

Ljubljana, Slovenia

Endocrinology Research Centre

🇷🇺

Moscow, Russian Federation

Dokuz Eylul University School of Medicine

🇹🇷

İzmir, Turkey

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