Characteristic/ Study ID (trial identifier) |
Endpoint | Time of measurement |
Ludvik 2002 | Glycaemic control (P) | 0, 1.5 months |
Serum insulin, C‐peptide or insulin sensitivity (S) | 0, 1.5 months | |
Serum cholesterol (S) | 0, 1.5 months | |
Weight (S) | 0, 1.5 months | |
Adverse events (O) | 0, 1.5 months | |
Ludvik 2004 | Glycaemic control (P) | 0, 2, 3 months |
Serum cholesterol and triglyceride (S) | 0, 2, 3 months | |
Adverse events (O) | 0, 2, 3 months | |
Ludvik 2008 | Glycaemic control (P) | 0, 5 months |
Serum cholesterol and triglyceride (S) | 0, 5 months | |
Adverse events (O) | 0, 5 months | |
Footnotes aEndpoint in bold/italic = review's primary/secondary outcome b(P) Primary or (S) secondary endpoint(s) refer to verbatim statements in the publication, (O) other endpoints relate to outcomes that were not specified as 'primary' or 'secondary' outcomes in the report |