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Trial - EUCTR2021-002014-14-CZ


Column Value
Trial registration number EUCTR2021-002014-14-CZ
Full text link
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

First author
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

Fakultní nemocnice Hradec Králové - Oddělení klinických hodnocení

Contact
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

karolina.mullerova@fnhk.cz

Registration date
Last imported at : June 26, 2022, 6 p.m.
Source : EU Clinical Trials Register

2021-04-16

Recruitment status
Last imported at : May 30, 2024, noon
Source : EU Clinical Trials Register

Completed

Study design
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

nonRCT

Allocation
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

Non-randomized

Design
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

Parallel

Masking
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

Open label

Center
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

single-center

Study aim
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

Prevention

Inclusion criteria
Last imported at : Nov. 26, 2021, 4 p.m.
Source : EU Clinical Trials Register

1. age 20 ≥ 75 years 2. the ability to understand the nature and course of the study and to agree in writing to the study by signing Informed Consent 3. Day 28 after dosing Moderna 4. with a functional kidney transplant 5. with stable function of the transplanted kidney (graft) 6. more than 3 months after kidney transplantation 7. no change in immunosuppressive therapy and / or no infection since the Moderna dose was given 1. věk 20 ≥ 75 let 2. schopnost porozumět podstatě a průběhu studie a písemně vyjádřit souhlas se studií podpisem Informovaného souhlasu 3. 28. den po aplikaci dávky vakcíny Moderna 4. s funkční transplantovanou ledvinou 5. se stabilní funkcí transplantované ledviny (štěpu) 6. více než 3 měsíce po transplantaci ledviny 7. beze změny imunosupresivní léčby a/nebo bez infekce v období od podání dávky vakcíny Moderna

Exclusion criteria
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

1. insufficient venous system in the upper limbs with the risk of having repeated intravenous injections to obtain a blood sample 2. past COVID-19 disease 3. concurrent participation in another clinical trial 4. pregnancy, breastfeeding 1. insuficientní žilní systém na horních končetinách s rizikem nutnosti opakovaných vpichů do žíly k získání vzorku krve 2. prodělané onemocnění COVID-19 3. souběžná účast v jiném klinickém hodnocení 4. gravidita, kojení

Number of arms
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

1

Funding
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

Fakultní nemocnice Hradec Králové

Inclusion age min
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

20

Inclusion age max
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

75

Countries
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

Czech Republic

Type of patients
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

High risk patients

Severity scale
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

N/A

Total sample size
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

60

primary outcome
Last imported at : Nov. 26, 2021, 4 p.m.
Source : EU Clinical Trials Register

To describe the antibody and cellular response in clinically stable patients after successful kidney transplantation 33 weeks after the second dose of the registered mRNA-vaccine against COVID-19 disease (Spikevax vaccine, Moderna), ie on the day of the third dose of vaccine. Popsat protilátkovou a buněčnou odpověď u klinicky stabilních pacientů po úspěšné transplantaci ledviny v odstupu 33 týdnů od aplikace druhé dávky registrované mRNA-vakcíny proti COVID-19 onemocnění (vakcína Spikevax, Moderna), tj. v den podání třetí dávky vakcíny.

Notes
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

nan

Phase
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

Phase 4

Arms
Last imported at : May 15, 2021, 1:30 a.m.
Source : EU Clinical Trials Register

[{"arm_notes": "1", "treatment_id": 824, "treatment_name": "Mrna-1273", "treatment_type": "Rna based vaccine", "pharmacological_treatment": "Vaccine"}]