Created at Source Raw Value Validated value
July 7, 2022, 1:30 p.m. oms

[{"arm_notes": "", "treatment_id": null, "treatment_name": "C01.748.214;C01.748.214;Group 1: a total of 233 participants who received two doses of primary vaccination (1st and 2nd doses) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); a full dose of the AstraZeneca/Fiocruz vaccine and will be followed in the study for six monthsGroup 2: a total of 233 participants who received two doses of primary vaccination (1st and 2nd dose) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); half a dose of the AstraZeneca/Fiocruz vaccine; and will be followed up in the study for six monthsGroup 3: a total of 234 participants who received two doses of primary vaccination (1st and 2nd dose) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); half a dose of the Pfizer/Wyeth vaccine; and will be followed up in the study for six months", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}, {"arm_notes": "", "treatment_id": null, "treatment_name": "Group 1: a total of 233 participants who received two doses of primary vaccination (1st and 2nd doses) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); a full dose of the AstraZeneca/Fiocruz vaccine and will be followed in the study for six months", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}, {"arm_notes": "", "treatment_id": null, "treatment_name": "Group 2: a total of 233 participants who received two doses of primary vaccination (1st and 2nd dose) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); half a dose of the AstraZeneca/Fiocruz vaccine; and will be followed up in the study for six months", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}, {"arm_notes": "", "treatment_id": null, "treatment_name": "Group 3: a total of 234 participants who received two doses of primary vaccination (1st and 2nd dose) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); half a dose of the Pfizer/Wyeth vaccine; and will be followed up in the study for six months", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}]

[{"arm_notes": "full dose, 1st and 2nd doses of the Sinovac", "treatment_id": 161, "treatment_name": "Chadox1 ncov-19", "treatment_type": "Non replicating viral vector", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "half dose, 1st and 2nd doses of the Sinovac", "treatment_id": 161, "treatment_name": "Chadox1 ncov-19", "treatment_type": "Non replicating viral vector", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "half dose, 1st and 2nd doses of the Sinovac", "treatment_id": 222, "treatment_name": "Bnt162b2", "treatment_type": "Rna based vaccine", "pharmacological_treatment": "Vaccine"}]

June 30, 2022, 4:30 p.m. oms

[{"arm_notes": "", "treatment_id": null, "treatment_name": "Group 1: a total of 233 participants who received two doses of primary vaccination (1st and 2nd doses) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); a full dose of the AstraZeneca/Fiocruz vaccine and will be followed in the study for six monthsGroup 2: a total of 233 participants who received two doses of primary vaccination (1st and 2nd dose) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); half a dose of the AstraZeneca/Fiocruz vaccine; and will be followed up in the study for six monthsGroup 3: a total of 234 participants who received two doses of primary vaccination (1st and 2nd dose) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); half a dose of the Pfizer/Wyeth vaccine; and will be followed up in the study for six months;C01.748.214;C01.748.214", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}, {"arm_notes": "", "treatment_id": null, "treatment_name": "Group 1: a total of 233 participants who received two doses of primary vaccination (1st and 2nd doses) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); a full dose of the AstraZeneca/Fiocruz vaccine and will be followed in the study for six months", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}, {"arm_notes": "", "treatment_id": null, "treatment_name": "Group 2: a total of 233 participants who received two doses of primary vaccination (1st and 2nd dose) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); half a dose of the AstraZeneca/Fiocruz vaccine; and will be followed up in the study for six months", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}, {"arm_notes": "", "treatment_id": null, "treatment_name": "Group 3: a total of 234 participants who received two doses of primary vaccination (1st and 2nd dose) of the Sinovac/Butantan vaccine will receive as a booster dose (3rd dose); half a dose of the Pfizer/Wyeth vaccine; and will be followed up in the study for six months;C01.748.214;C01.748.214", "treatment_type": "TODO", "pharmacological_treatment": "TODO"}]

[{"arm_notes": "", "treatment_id": 161, "treatment_name": "Chadox1 ncov-19", "treatment_type": "Non replicating viral vector", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "half dose", "treatment_id": 161, "treatment_name": "Chadox1 ncov-19", "treatment_type": "Non replicating viral vector", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "half dose", "treatment_id": 219, "treatment_name": "Bnt162", "treatment_type": "Rna based vaccine", "pharmacological_treatment": "Vaccine"}]