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Column | Value |
---|---|
Trial registration number | EUCTR2020-002009-25-CZ |
Full text link
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
https://www.clinicaltrialsregister.eu/ctr-search/trial/2020-002009-25/CZ |
First author
Last imported at : Sept. 16, 2022, 12:30 p.m. Source : EU Clinical Trials Register |
|
Contact
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
matejovic@fnplzen.cz |
Registration date
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
2020-06-04 |
Recruitment status
Last imported at : Sept. 15, 2022, noon Source : EU Clinical Trials Register |
Terminated |
Study design
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
RCT |
Allocation
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
Randomized |
Design
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
Parallel |
Masking
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
Blind label |
Center
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
single-center |
Study aim
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
Treatment |
Inclusion criteria
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
1. Adults (>18yrs of age) with confirmed COVID-19 disease who require hospital admission 2. Need for less than 8L/min of O2 via supplemental device to maintain SpO2 > 92% 3. Signed informed consent by patient 1. Dospělí (18 let a více) s potvrzenou nemocí COVID-19, kteří vyžadují hospitalizaci 2. Potřebují méně než 8L/min O2 prostřednictvím jakéhokoliv zařízení k udržení FiO2 > 92% 3. Podepsaný informovaný souhlas pacienta |
Exclusion criteria
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
1. Patients who require > 8L O2/min via a supplemental device to maintain SpO2>92% 2. Patients who are in shock as defined by vasopressor requirements 3. Patients with clear limitations of treatment (not for intubation) 4. Moribund patients 5. Pregnant patients 6. Known allergy to Eftilagimod Alpha, or L-Arginine 1. Pacienti, kteří potřebují > 8L O2/min prostřednictvím doplňkového zařízení k udržení SpO2>92% 2. Pacienti, kteří jsou v šoku - definováno požadavky na vasopresor 3. Pacienti s jasnými omezeními léčby (ne pro intubaci) 4. Umírající pacienti 5. Těhotné pacientky 6. Známá alergie na Eftilagimod Alpha, nebo L-arginin |
Number of arms
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
2 |
Funding
Last imported at : Sept. 16, 2022, 12:30 p.m. Source : EU Clinical Trials Register |
Fakultní nemocnice Plzeň |
Inclusion age min
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
19 |
Inclusion age max
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
100 |
Countries
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
Czech Republic |
Type of patients
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
Moderate/severe disease at enrollment |
Severity scale
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
4: Moderate/severe disease at enrollment |
Total sample size
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
104 |
primary outcome
Last imported at : Sept. 16, 2022, 12:30 p.m. Source : EU Clinical Trials Register |
patient's clinical status (on a 7-point ordinal scale) at day 15 as per an adapted WHO recommended study protocol. 1. Not hospitalized, 2. Hospitalized, not requiring supplemental oxygen 3. Hospitalized, requiring supplemental oxygen 4. Hospitalized, on high flow oxygen device 5. Hospitalized in ICU, on non-invasive ventilation 6. Hospitalized in ICU, on invasive mechanical ventilation or ECMO 7. Death klinický stav pacienta (v 7-bodové řadové stupnici) v den 15 podle upraveného protokolu doporučeného WHO. 1. Nehospitalizován 2. Hospitalizován, nevyžaduje doplňkový kyslík 3. Hospitalizován, vyžadující doplňkový kyslík 4. Hospitalizován, na vysokoprůtokovém kyslíkovém zařízení 5. Hospitalizován na JIP, na neinvazivní ventilaci 6. Hospitalizován na JIP, na invazivní mechanické ventilaci nebo ECMO 7. Smrt |
Notes
Last imported at : Sept. 16, 2022, 12:30 p.m. Source : EU Clinical Trials Register |
TODO |
Phase
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
Phase 2 |
Arms
Last imported at : Nov. 27, 2020, 1:30 a.m. Source : EU Clinical Trials Register |
[{"arm_notes": "", "treatment_id": 450, "treatment_name": "Eftilagimod alpha", "treatment_type": "Other targeted therapies", "pharmacological_treatment": "Pharmacological treatment"}, {"arm_notes": "", "treatment_id": 2187, "treatment_name": "Placebo", "treatment_type": "Placebo", "pharmacological_treatment": "Placebo"}] |