Nephrogenic Systemic Fibrosis (NSF): Analysis of Tissue Gadolinium Levels
Completed
Conditions studied: Nephrogenic Systemic Fibrosis, Nephrogenic Fibrosing Dermopathy
In brief
The primary objective of this study is to determine any causative or associated factors for the development of Nephrogenic Systemic Fibrosis (NSF), Nephrogenic Fibrosing Dermopathy (NFD), or related diagnosis. Our primary focus will be on the previous administration of gadolinium to these patients, but we will also look at other postulated causes and risk factors. The secondary objective of this study is to assess tissue gadolinium (Gd) levels in five groups of subjects: * Those affected by NSF. * Those with normal kidney function who have undergone a medical imaging procedure using Gd-based contrast agent (GBCA) in the 2 years prior to a skin biopsy. * Those with normal kidney function who have never been exposed to GBCA and have had a skin biopsy. * Those on dialysis or with eGFR ≤ 30 ml/min/1.73 m2 who have had a medical imaging procedure using GBCA in the 2 years prior to skin biopsy. * Those on dialysis or with eGFR ≤ 30 ml/min/1.73 m2 who have never been exposed to GBCA and have had skin biopsy. We hypothesize that there is a correlation between the administration of Gd-containing agents usually associated with MRI procedures and the development of NSF in those with renal failure and some other predisposing condition. We also hypothesize that tissue Gd levels in those with NSF will be higher than in those who have been exposed to GBCA but do not have NSF. Of the two groups without NSF but with exposure to GBCA, we hypothesize that those with kidney dysfunction will have higher tissue Gd levels than those with normal kidney function. We hypothesize that in the two groups of subjects without exposure to GBCA, there will be no detectable levels of Gd, regardless of kidney function status.
Key facts
- Study ID
- NCT01014754
- Run by
- Northwestern University
- People needed
- 24
- Starts
- 2007-08-01
- Expected to finish
- 2014-06-01
- Last updated by the study team
- 2014-12-04
Who can join
Age: any. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Biopsy-confirmed diagnosis of NSF
You may not qualify if…
- Does not have NSF
- Normal renal plus gadolinium exposure
- Inclusion Criteria:
- eGFR >30
- Existing skin tissue sample
- Gadolinium exposure in 2 years preceding skin biopsy
- Exclusion Criteria:
- Does not fit inclusion criteria
- Abnormal renal plus gadolinium exposure
- Inclusion Criteria:
- eGFR <30 or on dialysis
- Existing skin tissue sample
- Gadolinium exposure in 2 years preceding skin biopsy
- Exclusion Criteria:
- Does not fit inclusion criteria
- Abnormal renal without gadolinium exposure
- Inclusion Criteria:
- eGFR <30 or on dialysis
- Existing skin tissue sample
- No gadolinium exposure ever
- Exclusion Criteria:
- Does not fit inclusion criteria
- Normal renal without gadolinium exposure
- Inclusion Criteria:
- eGFR >30
Where it is running
- Northwestern University Feinberg School of Medicine, Department of Dermatology — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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