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Column | Value |
---|---|
Trial registration number | IRCT20131221015878N3 |
Full text link
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
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First author
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
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Contact
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
biglari63@hotmail.com |
Registration date
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
2022-01-18 |
Recruitment status
Last imported at : April 10, 2022, 10:41 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Completed |
Study design
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
nonRCT |
Allocation
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Non-randomized |
Design
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Parallel |
Masking
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Open label |
Center
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
single-center |
Study aim
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Prevention |
Inclusion criteria
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Signed informed written consent Able to follow the vaccination schedules, visits and tests General health and controlled underlying diseases (based on the physician's recommendation) Iranian citizenship Resident in Tehran Both sexes (male and female) Aged above 18 years Receiving 2 doses of Sinopharm vaccine with 28±5 days interval Receiving 2 doses of Astrazeneca vaccine with 3 to 4 months interval All candidates whose second vaccination either Sinopharm or Astrazeneca was done 3 to 6 prior to enrollment. |
Exclusion criteria
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Having a history of vaccination against Covid-19 with other available vaccines History of COVID-19 based on laboratory or clinical evidence after receiving the vaccine History of any vaccinations except COVID-19 within 3 months prior to enrollment Pregnant or breastfeeding women or those who intend to become pregnant up to 3 months after the booster dose injection. Having uncontrolled hypertension (cytological pressure greater than 140 or diastolic pressure greater than 90 mm Hg) History of receiving blood or blood products such as immunoglobulin in the last three months Suffering from chronic kidney disease (GFR less than 30) Suffering from chronic liver disease (liver enzymes more than 5 times normal: 150ALT≥, 100AST≥) Suffering from uncontrolled asthma (Having had an asthma attack in the last three months) History of severe allergic reaction (anaphylaxis) to the vaccine during a person's lifetime History of treatment with immunosuppressive drugs 1 month before the booster injection (including oral and inhaled steroids (does not include topical steroids), cytostatic, interferon, immunoferon, transfer factor, Biomodulin T, any type of gammaglobin, levamisole , Heberferon, thymosin or any other immunomodulatory drug (including patients taking the above drugs due to an underlying disease). Having a fever or acute illness during the 7 days before the injection or on the day of the booster injection Suffering from an unstable heart disease |
Number of arms
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
5 |
Funding
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Pasture Institute of Iran |
Inclusion age min
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
18 |
Inclusion age max
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
80 |
Countries
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Iran |
Type of patients
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Healthy volunteers |
Severity scale
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
N/A |
Total sample size
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
190 |
primary outcome
Last imported at : Feb. 2, 2022, 1:11 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Increased Anti-Spike headline Quadrupling the neutralizing antibody titer |
Notes
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
|
Phase
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
Not reported |
Arms
Last imported at : Jan. 19, 2022, 1 p.m. Source : Iranian Registry of Clinical Trials (IRCT) |
[{"arm_notes": "1;received 2 first doses of Sinopharm", "treatment_id": 515, "treatment_name": "Finlay-fr-2 anti-sars-cov-2 vaccine", "treatment_type": "Protein subunit", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "1;received 2 first doses of Astrazeneca", "treatment_id": 515, "treatment_name": "Finlay-fr-2 anti-sars-cov-2 vaccine", "treatment_type": "Protein subunit", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "1;received 2 first doses of Sinopharm", "treatment_id": 184, "treatment_name": "Bbibp-corv", "treatment_type": "Inactivated virus", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "1;received 2 first doses of Astrazeneca", "treatment_id": 161, "treatment_name": "Chadox1 ncov-19", "treatment_type": "Non replicating viral vector", "pharmacological_treatment": "Vaccine"}, {"arm_notes": "1;received 2 first doses of Astrazeneca", "treatment_id": 515, "treatment_name": "Finlay-fr-2 anti-sars-cov-2 vaccine", "treatment_type": "Protein subunit", "pharmacological_treatment": "Vaccine"}] |