Van Vollenhoven 1999.
Methods | double blind RCT 6 months | |
Participants | Total: 19 Sex: male or female (only 3 male) Ethnicity: 33‐40% Caucasian; 11‐20% African‐American; 40‐44% other Median age:35‐39 yr Inclusion criteria: severe SLE Exclusion criteria: | |
Interventions | Grp 1: DHEA 200mg/dy Grp 2: placebo | |
Outcomes | Stated primary: stabilise major lupus manifestation SLEDAI, SLAM, HRQoL, renal proteinuria, biological SLEDAI, Prednisolone dose, Patient global VAS, Physician global VAS, Bone mineral density, other biochemical markers |
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Notes | Funding: NIH grant | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Unclear risk | B ‐ Unclear |
HRQoL ‐ health related quality of life including SF36 and Patient Visual analogue scores