Studies of Children With Metabolic and Other Genetic Disorders
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|ClinicalTrials.gov Identifier: NCT00025870|
Recruitment Status : Completed
First Posted : October 28, 2001
Last Update Posted : November 4, 2019
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This study will provide medical evaluations for patients with known or suspected metabolic and genetic disorders. It will allow NICHD investigators and trainees experience in diagnosing, managing, and treating patients with metabolic and genetic disorders who may not be eligible for an active NIH research trial. Participants in this protocol will only have tests and procedures used in the standard practice of medicine; there will be no experimental tests or treatments. Patients who are found eligible for an active research protocol will be offered participation in that study. The medical evaluations in this trial may uncover new disease processes that prompt new research initiatives.
People of all ages with a suspected or diagnosed genetic or metabolic condition may be eligible for this study. In addition, children with unexplained developmental delay, deafness, dysmorphism, congenital malformations, acidosis, failure to thrive, feeding problems, short stature, birth defects, and other syndromes of unknown cause may qualify.
Participants will have a medical history, including a family history, with possible review of previous medical records, and a physical examination. Other procedures may include:
- Consultation with medical specialists.
- Hearing and/or vision tests.
- Imaging studies, such as X-rays, ultrasound and magnetic resonance imaging (MRI).
- Blood drawing Blood samples (2 to 4 tablespoons from adults and 1 to 2 tablespoons from children) may be used for routine lab tests, genetic study, and other research purposes.
- Cheek swab DNA may be obtained by a cheek swab. A small brush is rubbed against the inside of the cheek to collect some cells.
- Skin biopsy Under local anesthetic, a small circle of skin (about 1/8-inch) is removed with a sharp cutting instrument similar to a cookie cutter.
- Muscle biopsy Under local anesthetic, a small piece of muscle tissue is removed to aid in diagnosis.
Participants will undergo only diagnostic procedures that are clinically indicated; that is, only tests needed to confirm or rule out a diagnosis will be done. Tissue samples collected for diagnostic purposes may also be used to obtain DNA for genetic studies and to establish cell lines (cells grown in the laboratory to be maintained indefinitely) for future research.
The results of the medical evaluation may indicate whether or not the participant has the disease that runs in the family (if a genetic disorder is indeed confirmed). Unless he or she requests otherwise, the subject (and parent in the case of a minor) will receive counseling regarding the test results. The implications of a positive test result will be explained, specifically, the participant s risk of having the disease, and the risk of passing the condition on to offspring.
|Condition or disease|
|Genetic Disorder Metabolic Disease|
|Study Type :||Observational|
|Actual Enrollment :||1090 participants|
|Official Title:||Studies of Pediatric Patients With Metabolic or Other Genetic Disorders|
|Study Start Date :||October 25, 2001|
|Study Completion Date :||June 23, 2016|
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
|Ages Eligible for Study:||up to 18 Years (Child, Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- INCLUSION CRITERIA:
- Patients with suspected or diagnosed genetic and/or metabolic conditions of all ages are eligible for this protocol.
- In addition, children with unexplained developmental delay, deafness, dysmorphism, congenital malformations, acidosis, failure to thrive, feeding problems, short stature, birth defects, and other syndromes of sporadic or unknown etiology will qualify for this protocol.
- The actual selection of patients most appropriate for research and clinical training needs will be made by protocol investigators.
- Patients that their care requires resources not available at the NIH Clinical Center will not be eligible for the in-patient part of this study.
- There are no exclusions for the out-patient or DNA collection part of the study.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00025870
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike|
|Bethesda, Maryland, United States, 20892|
|Principal Investigator:||Margarita J Raygada, Ph.D.||Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)|
|Responsible Party:||Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)|
|Other Study ID Numbers:||
|First Posted:||October 28, 2001 Key Record Dates|
|Last Update Posted:||November 4, 2019|
|Last Verified:||June 23, 2016|
Genetic Diseases, Inborn