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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00916838
Other study ID # 02-1012 -201102446
Secondary ID R01DK064832
Status Completed
Phase
First received
Last updated
Start date January 2003
Est. completion date February 2017

Study information

Verified date June 2018
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

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)

Study Design


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Washington University School of Medicine National Institutes of Health (NIH)
See also
  Status Clinical Trial Phase
Completed NCT00879203 - Glycemic Control, Brain Structure and Cognition in Youth With Type 1 Diabetes (T1DM) N/A

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