Type 1 Diabetes Mellitis Clinical Trial
— HYPOOfficial title:
Neurocognitive Impact of Hypoglycemia in Type 1 Diabetes
Verified date | June 2018 |
Source | Washington University School of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
125 children with Type 1 Diabetes mellitis (T1DM) between 4 and 16 were recruited and 62
healthy siblings also enrolled in the study.
Children with T1DM and sibling controls ages 4 to 16 were assessed on memory and executive
control skills at entry to the study (Test 1) and after two years of close monitoring for
blood sugar events (Test 2). Diabetic children have their blood sugar tested directly before
and after cognitive testing to ensure their blood sugar is within range during the testing.
The 2-year follow-up period involves parents/child reporting any severe diabetic episode and
periodically providing the results of the diabetic child's usual blood tests from their
glucose monitoring device.
Children 7 and older also underwent high resolution MRI scans.
Status | Completed |
Enrollment | 187 |
Est. completion date | February 2017 |
Est. primary completion date | March 2006 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 4 Years to 16 Years |
Eligibility |
Inclusion Criteria: - Age 4 - 16 (for MRI, must be 7 or older) Exclusion Criteria: - Pregnant or lactating (females 13+) - Chronic disease other than T1DM, well-controlled asthma, or Hashimoto's thyroiditis. (Exclude for hypothyroidism) - Other current serious medical illness - Co-morbid psychiatric illness: such as mania, ADHD, LD, major depression, mental retardation, or psychoactive drug dependence - Co-morbid neurological illness: stroke, seizure, major loss of consciousness, other brain trauma/surgery, or head injuries (i.e. near drowning), encephalitis, or hydrocephalus, blindness, deafness - EXCEPT T1DM-related - Pre-maturity at birth >4 wks early (<36 wk term) w/ sequelae e.g. on respirator at NICU - Use of psychoactive medications or exposure to neuroleptics (except that exposures of less than 1 month, occurring more than 5 years ago, will be allowed) or pts. w/recent tx w/dopamine depleting agents or stimulants such as Ritalin, Cylert, Adderall - Contraindication to MRI scan (e.g. claustrophobia, metal implants, foreign bodies) - N/A if < 4 years old - Full set (top and bottom) orthodontic braces. (Half set braces, fillings, and retainers are OK) |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Washington University School of Medicine | National Institutes of Health (NIH) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00879203 -
Glycemic Control, Brain Structure and Cognition in Youth With Type 1 Diabetes (T1DM)
|
N/A |