Hartkamp 2004.
Methods | Double blind, controlled trial (Probably randomised but does not specify) 12 months | |
Participants | Total: 60 Sex: female Ethnicity: 82‐93% Caucasian Median age: 41‐45 years Inclusion criteria: quiescent SLE, on <10mg prednisolone Exclusion criteria: nil else | |
Interventions | Grp 1: DHEA 200mg/dy Grp 2: placebo | |
Outcomes | Stated primary: Wellbeing and fatigue (not reported) SLEDAI, Bone mineral density |
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Notes | Funding: Dutch Arthritis Association | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Unclear risk | B ‐ Unclear |