Row |
Data |
Results |
Booster |
Placebo |
1 |
1st author |
|
2 |
Date of publication |
|
3 |
Design of clinical trial |
Randomised clinical trial |
|
Quasi‐randomised study |
|
4 |
Follow‐up time from last vaccination (year) |
|
5 |
Endemicity |
High |
|
Intermediate |
|
Low |
|
6 |
Participants |
General population |
|
Healthcare workers |
|
Intravenous (IV) drug abusers |
|
Sex partners |
|
Others |
|
7 |
Mean age (year) |
|
|
8 |
Vaccine schedule |
3‐dose |
|
4‐dose |
|
9 |
Initial vaccine type |
Recombinant vaccine (RV) |
|
Plasma derived vaccine (PDV)? |
|
10 |
Proportion with response to initial vaccination (%) |
|
|
11 |
Booster type |
Recombinant vaccine (RV) |
|
|
Plasma derived vaccine (PDV)? |
|
|
12 |
Booster dosage (mcg) |
|
|
13 |
Injection site |
Deltoid |
|
Thigh |
|
Gluteus |
|
14 |
Injection route |
IM |
|
ID |
|
SD |
|
15 |
Sample size |
|
|
16 |
Dropouts |
|
|
17 |
Anamnestic immune response (AIR) |
|
|
18 |
Proportion of anamnestic immune response (PAIR) |
|
|
19 |
Before intervention (booster) |
GMT (mIU/mL) |
|
|
95% CI of GMT |
|
|
20 |
1 week after intervention (booster) |
GMT (mIU/mLl) |
|
|
95% CI of GMT |
|
|
21 |
2 weeks after booster dose (booster) |
GMT (mIU/mL) |
|
|
95% CI of GMT |
|
|
22 |
3 weeks after intervention (booster) |
GMT (mIU/mL) |
|
|
95% CI of GMT |
|
|
23 |
4 weeks after intervention (booster) |
GMT (mIU/mL) |
|
|
95% CI of GMT |
|
|
24 |
2 months after intervention (booster) |
GMT (mIU/mL) |
|
|
95% CI of GMT |
|
|
25 |
1 year after intervention (booster) |
GMT (mIU/mL) |
|
|
95% CI of GMT |
|
|
26 |
Adverse events of booster |
Local |
Pain |
|
|
Tenderness |
|
|
Redness |
|
|
Swelling |
|
|
Other |
|
|
Systemic |
Fever |
|
|
Headache |
|
|
Malaise |
|
|
Irritability |
|
|
Rash |
|
|
Nausea |
|
|
Myalgia |
|
|
Arthralgia |
|
|
Other |
|
|