Chronic Granulomatous Disease Clinical Trial
Official title:
Cognitive Function in Leukocyte Disorders
This study will try to determine what causes learning, behavioral and emotional problems in
children with chronic granulomatous disease (GCD) and other phagocyte disorders. (Phagocytes
are a type of white blood cell.) Children with these disorders have frequent severe
infections that require hospitalization, sometimes for long periods of time. Many of them
also have problems with school, learning, behavior, anxiety and depression. This study will
explore whether these latter problems are a direct result of the illness itself or are a
consequence of frequent, long hospitalizations, or are due to other factors. Test findings
in these children will be compared with those of children with cystic fibrosis-another
disease that causes frequent infections requiring prolonged hospitalization.
Patients age 2 or older with GCD or other phagocytic disorders or cystic fibrosis may be
eligible for this study. Participants (or a parent or guardian) will complete questionnaires
including personal information such as age, gender and marital status, a family medical
history, and information on their illness. Patients will be given various psychological and
intelligence tests, and they and their parents or guardians will be interviewed by a child
psychiatrist. The tests and interviews take a total of about 5 hours and are given in two or
three separate sessions.
The tests may reveal problems such as learning disorders, attention-deficit hyperactivity
disorder, anxiety, or depression. If any of these problems are identified, appropriate
referrals will be made for specialized services, such as special school placement, tutoring,
or counseling.
Status | Completed |
Enrollment | 150 |
Est. completion date | July 2005 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
INCLUSION CRITERIA Presence of a confirmed diagnosis of CGD or other phagocytic disorder. Age 2 or older. English spoken in the home. EXCLUSION CRITERIA Unconfirmed phagocytic disorder. Under age 2. First language is other than English. |
N/A
Country | Name | City | State |
---|---|---|---|
United States | National Institute of Allergy and Infectious Diseases (NIAID) | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Institute of Allergy and Infectious Diseases (NIAID) |
United States,
Batshaw ML. Mental retardation. Pediatr Clin North Am. 1993 Jun;40(3):507-21. Review. — View Citation
Boyle IR, di Sant'Agnese PA, Sack S, Millican F, Kulczycki LL. Emotional adjustment of adolescents and young adults with cystic fibrosis. J Pediatr. 1976 Feb;88(2):318-26. — View Citation
Eliez S, Reiss AL. Genetics of childhood disorders: XI. Fragile X syndrome. J Am Acad Child Adolesc Psychiatry. 2000 Feb;39(2):264-6. — View Citation
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT03278912 -
Natural History of Intestinal Inflammation in People With Primary Immune Dysregulations
|
||
Recruiting |
NCT01652092 -
Allogeneic Hematopoietic Stem Cell Transplant for Patients With Primary Immune Deficiencies
|
N/A | |
Completed |
NCT04136028 -
IL-1 Receptor Inhibitor for Granulomatous Complications in Patients With Chronic Granulomatous Disease
|
Early Phase 1 | |
Recruiting |
NCT05687474 -
Baby Detect : Genomic Newborn Screening
|
||
Terminated |
NCT03080480 -
Pioglitazone Therapy for Chronic Granulomatous Disease
|
Phase 1/Phase 2 | |
Terminated |
NCT00394316 -
Gene Therapy for Chronic Granulomatous Disease
|
Early Phase 1 | |
Recruiting |
NCT03910452 -
Haploidentical Transplant for People With Chronic Granulomatous Disease (CGD) Using Alemtuzumab, Busulfan and TBI With Post-Transplant Cyclophosphamide
|
Early Phase 1 | |
Terminated |
NCT02282904 -
Haploidentical Transplant for People With Chronic Granulomatous Disease Using Post Transplant Cyclophosphamide
|
Phase 1/Phase 2 | |
Terminated |
NCT02926963 -
Generation of Powerful Biological Tools for Understanding the Pathophysiology of Chronic Granulomatous Disease.
|
N/A | |
Completed |
NCT00006417 -
Modified Stem Cell Transplantation Procedure for Treating Chronic Granulomatous Disease
|
Phase 2 | |
Completed |
NCT00368446 -
Genetic Disorders of Mucociliary Clearance in Nontuberculous Mycobacterial Lung Disease
|
||
Enrolling by invitation |
NCT03655223 -
Early Check: Expanded Screening in Newborns
|
||
Recruiting |
NCT06162936 -
Neutrophil Oxidative Burst in Early and Late Onset Pediatric Inflammatory Bowel Disease
|
||
Terminated |
NCT05915897 -
Whole Blood Biospecimen Collection for Subjects With Chronic Granulomatous Disease (CGD)
|
||
Terminated |
NCT00325078 -
Infliximab to Treat Crohn'S-like Inflammatory Bowel Disease in Chronic Granulomatous Disease
|
Phase 1/Phase 2 | |
Completed |
NCT00001317 -
A Phase IV Study of Recombinant Human Gamma Interferon in Patients With Chronic Granulomatous Diseases of Childhood
|
Phase 4 | |
Completed |
NCT03548818 -
Role of Interferon-gamma 1-b (IFN-γ) on Cells of the Innate Immune System: Functional, Biochemical and Gene Expression Studies in Patients With Chronic Granulomatous Disease
|
||
Recruiting |
NCT01821781 -
Immune Disorder HSCT Protocol
|
Phase 2 | |
Completed |
NCT00578643 -
Matched Unrelated or Non-Genotype Identical Related Donor Transplantation For Chronic Granulomatous Disease
|
Phase 2 | |
Terminated |
NCT00006054 -
Allogeneic Bone Marrow Transplantation in Patients With Primary Immunodeficiencies
|
N/A |