Studies of Heritable Disorders of Connective Tissue
Completed
Conditions studied: Ehlers-Danlos Syndrome, Stickler Syndrome, Marfan Syndrome
In brief
Background: \- Heritable disorders of connective tissue are genetic conditions that can affect the skin and other parts of the body. They are related to mutations in genes that are responsible for building tissues. The symptoms differ among disorders. Researchers want to study which genes may be responsible for different disorders. They will be performing a long-term (up to 10 years) study and a study that requires a single visit. These studies will look at how these disorders affect the body and what genes may cause these conditions. Objectives: \- To perform one-time and long-term studies of people who have heritable disorders of connective tissue. Eligibility: \- Individuals at least 2 years of age who have or may have a heritable disorder of connective tissue. Design: * Participants will be screened with a physical exam, medical history, and blood samples. * Participants will be on one of two parts of this study. The longitudinal arm will require long-term study over about 10 years. The mutational analysis arm will involve a single visit. * Longitudinal arm participants must be at least 12 years of age. They will have study visits at regular intervals for up to 10 years. The tests given at these visits may include all or some of the following: * Blood, saliva, urine, and skin samples * Heart and lung function tests * Magnetic resonance imaging scans of the neck, chest, spine, and abdomen * Other imaging studies such as x-rays, bone density scans, and ultrasounds * Questionnaires about sleep, pain, and quality of life * Photographs of affected areas. * Mutational analysis arm participants will have a single study visit. They will provide blood and saliva samples. They will provide tissue from a skin biopsy. They will also let the researchers take photos of any affected body parts. They will complete questionnaires about sleep, pain, and quality of life.
Key facts
- Study ID
- NCT00270686
- Run by
- National Institute on Aging (NIA)
- People needed
- 929
- Starts
- 2003-01-21
- Expected to finish
- 2015-01-02
- Last updated by the study team
- 2018-04-05
Who can join
Age: 2 and older. Sex: any. Healthy volunteers: accepted.
You may not qualify if…
- The only exclusion criterion is inability to provide informed consent, or the absence of a guardian who is authorized to provide informed consent in the case of minor subjects.
- There will be no exclusion based upon age, gender, ethnicity, socioeconomic status, or any other factor except ability to provide informed consent.
- Pregnant and nursing women may be limited in their participation in some aspects of the study (e.g. ionizing radiation exposure or MRI) during the time that they are pregnant or nursing.
Where it is running
- National Institute of Aging, Clinical Research Unit — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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