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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01330368
Other study ID # 10-007747
Secondary ID
Status Completed
Phase N/A
First received December 14, 2010
Last updated September 29, 2017
Start date October 2010
Est. completion date June 2017

Study information

Verified date September 2017
Source Children's Hospital of Philadelphia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to compare healthy children to children who have systemic lupus erythematosus (SLE). SLE is a childhood disease that has high risk for low bone mass and vertebral compression fractures.


Description:

The purpose of this research study is to measure bone mass in children with SLE using different measurement techniques. Children with chronic illnesses are at risk of bone fragility. This is important because bone fragility can result in childhood fractures especially children with SLE. Therefore better diagnosis technique can lead to better management of bone health.


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date June 2017
Est. primary completion date July 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 21 Years
Eligibility Inclusion Criteria:

- For SLE subjects: Subjects age 5-21 drawn from rheumatology clinic at Children's Hospital of Philadelphia diagnosed with SLE for at least 1 month. Also subjects with no known vertebral compression fracture of L2.

- For Control subjects: Subjects age 5-21. Controls will be a 50% male/female.

Exclusion Criteria:

- For SLE subjects: Subjects with SLE will be excluded if they have conditions or drug exposure unrelated to SLE and known to impact growth or bone health.

- For Control subjects: Chronic disease or syndrome known to affect growth or bone health, prematurity (<37 weeks gestation), or use of any medication known to affect growth.

Study Design


Locations

Country Name City State
United States The Children's Hospital of Philadelphia Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Children's Hospital of Philadelphia

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Age and sex specific z-scores for lumbar spine (L2) volumetric bone mineral density (BMD) (trabecular and total) and vertebral volume. 2 years
Secondary Mean lumbar spine stiffness and strength in children with SLE and healthy controls correlation between standard and low dose lumbar spine. 2 years
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