4 Octubre 2023 - 12:11pm por FINLAY | 5 Octubre 2023 - 10:07am por FINLAY | ||
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Cambios a Date of first enrollment | |||
- | 2023-10-04 00:00:00 | + | 2023-10-09 00:00:00 |
Cambios a Primary outcome(s) | |||
- | 1.Proportion of adverse events attributable to vaccination with VCN7-T 30 days after each dose (Frequency and proportion of adverse events reported after the application of each dose of the evaluated schemes). Measurement time: From inoculation until the following 30 days.
| + | Proportion of adverse events attributable to vaccination with VCN7-T, 30 days after vaccination. |
- | 2.Proportion of solicited adverse events attributable to vaccination with VCN7-T up to 7 days after administration of each dose (Frequency and proportion of adverse events reported after the application of each dose of the evaluated schemes). Measurement time: From inoculation until the following 7 days. | + | |
Cambios a Key secondary outcomes | |||
- | 1. Cumulative incidence of pneumonia and IPD cases (Rates of pneumonia and IPD recorded after immunization). Measurement time: From inoculation until the following 2 years.
| + | 1. Cumulative incidence of pneumonia and IPD cases.
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- | 2.Percentage of subjects in the subgroup studied, with an immune response to the vaccine serotypes (Stratified randomization by age and underlying diseases most representative in the sample; sampling of 5 ml of blood pre- and post-vaccination from a subgroup of 200 subjects). Measurement time: T0 (before inoculation of the vaccine candidate); T28 (28 days after inoculation of the vaccine candidate).
| + | 2. Percentage of subjects in the studied subgroup, with an immune response to the vaccine serotypes. |
- | + | ||
Cambios a Inclusion criteria | |||
- | 1. Patients over one year old included in the risk groups defined in the health areas of the province of Havana.
| + | 1. Patients from 1 to 18 years of age, of any sex, from the province of Havana, identified in risk groups for pneumococcal disease.
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- | 2. Informed consent of parents and assent of adolescents for vaccination and follow-up.
| + | 2. Informed consent of parents and assent of adolescents for vaccination and follow-up. |
- | + | ||
Cambios a Exclusion criteria | |||
1. Previous pneumococcal vaccination.
| 1. Previous pneumococcal vaccination.
| ||
- | 2. Children with a referred allergy to thiomersal or any biological product or vaccines causing a serious adverse reaction such as anaphylaxis.
| + | 2. Children with a reported allergy to thiomersal or any biological product or vaccines causing a serious adverse reaction of the anaphylaxis type.
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- | 3. Decompensation of the underlying disease at the time of evaluation
| + | 3. Decompensation of the underlying disease at the time of evaluation.
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- | 4. Acute infectious diseases | + | 4. Subjects with febrile or acute infectious illness at the time of application of the vaccine candidate, or in the previous 7 days.
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+ | 5. Subjects vaccinated according to the Cuban immunization schedule, in a period of less than 15 days prior to the application of the investigational product.
| ||
+ | 6. Adolescents who are pregnant or have amenorrhea greater than 4 weeks before the application of the vaccine candidate. | ||
Cambios a Record Verification Date | |||
- | 2023/10/04 | + | 2023/10/05 |
Cambios a Next update date | |||
- | 2024/10/04 | + | 2024/10/05 |
Revisión de 5 Octubre 2023 - 10:07am