Ref (type) | Population | Outcome, Interventions | Results and statistical analysis | Effect size | Favours |
Adverse effects | |||||
RCT Crossover design 3-armed trial |
22 people In review |
Adverse effects (not further detailed)
10/22 (45%) with nifedipine 10 mg 16/22 (72%) with nifedipine 20 mg 6/22 (27%) with placebo |
Significance not assessed |
||
RCT Crossover design |
26 people In review |
Adverse effect
16/21 (76%) with nifedipine Not reported with placebo |
|||
RCT |
Number of people not reported In review |
Oedema
24% with nifedipine 0% with placebo |
P = 0.01 |
Effect size not calculated | placebo |
RCT |
Number of people not reported In review |
Flushing
8% with nifedipine 0% with placebo |
P = 0.01 |
Effect size not calculated | placebo |
RCT |
Total number of people not reported In review |
Tachycardia
2 people with nifedipine 0 people with placebo |
Significance not assessed |
||
RCT |
39 people In review |
Overall adverse effects
with nifedipine with placebo Absolute results not reported |
Reported as not significant P value not reported |
Not significant | |
RCT |
39 people In review |
Palpitations
7/18 (39%) with nifedipine 1/18 (6%) with placebo |
P <0.05 |
Effect size not calculated | placebo |
RCT Crossover design |
23 people In review |
Adverse effects (post-crossover results)
14/23 (61%) with nifedipine 2/23 (9%) with placebo |
P = 0.05 |
Effect size not calculated | placebo |
RCT Crossover design |
34 people In review |
Adverse effects (post-crossover results)
12 weeks
26/34 (76%) with nifedipine 5/34 (15%) with placebo |
Significance not assessed |