MacLeod 1995.
Methods | Trial design: Crossover study Randomisation procedure: Data missing Allocation concealment: Adequate Blinding: Double‐blind | |
Participants | Country: UK Setting: Single centre Number: 40 Type of diabetes: Type 1 Mean age [years]: 30 Mean diabetes duration [years]: N/A Other characteristics: Subgroup of patients with longer duration of diabetes | |
Interventions | Type of human insulin: Semi‐synthetic Type of animal insulin: Purified porcine Duration of trial [months]: 3 | |
Outcomes | 1.HbA1c [%]: ‐ 2.HbA1 [%]: 8.7±2.0 vs 8.6±2.4 (hum. vs anim.) 3.Fasting plasma glucose [mmol/L] ‐ 4.Insulin dose [Units/day]: ‐ 5.Insulin antibodies [%]: ‐ 6.Adverse effects: ‐ | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Low risk | A ‐ Adequate |