v3.0.7
Please consider this website is continuously evolving and still under development
to harmonize automatic data extraction and integrate manual data annotation.
Column | Value |
---|---|
Trial registration number | EUCTR2020-005863-29-IT |
Full text link
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
https://www.clinicaltrialsregister.eu/ctr-search/trial/2020-005863-29/IT |
First author
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
|
Contact
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
sophia.campbell@asst-fbf-sacco.it |
Registration date
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
2021-08-17 |
Recruitment status
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Recruiting |
Study design
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
RCT |
Allocation
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Randomized |
Design
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Parallel |
Masking
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Blind label |
Center
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
multi-center |
Study aim
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Treatment |
Inclusion criteria
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
- Age 18 years or older, - Positive molecular COVID-19 test on nasopharyngeal swab, - Interstitial pneumonia confirmed on lung CT scan, - Indication to helmet cPAP according to the COVID-19 Treatment Guideline criteria (21), i.e. the presence of at least one of the following signs during O2 therapy with O2 mask reservoir-bag 15 L/min: SpO2 < 92% and respiratory rate > 26/min and/or evident respiratory distress (point 5 on the WHO ordinal scale). - Età maggiore di 18 anni, - Tampone molecolare COVID-19 positivo, - Diagnosi di polmonite interstiziale confermato da TAC polmonare, - Indicazione a ventilazione non invasiva cPAP mediante casco secondo il criterio di mancata risposta a ossigeno terapia con O2 mask reservoir-bag 15 L/min intesa come: SpO2 < 92% e frequenzarespiratoria > 26/min e/o insufficienza respiratoria evidente (punteggio 5 sulla scala OMS). |
Exclusion criteria
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
- Age 80 years or older, - Ongoing anticoagulant therapy, - Clinically not compatible with helmet cPAP interruption for 10-25 minutes 4 times a day, - Home cPAP treatment, - Home O2 therapy, - Insulin-dependent diabetes mellitus - Acute myocardial infarction during the previous 6 months, - Ongoing oncological disease, - Chronic renal failure, - CT scan diagnosis of pulmonary thromboembolism, - Body Mass Index (BMI) over 40, - Uncontrolled bleeding, - Not able to understand or sign the informed consent. - Età maggiore o uguale a 80 anni, - Terapia anticoagulante in corso, - Clinicamente non compatibile con interruzione del trattamento con cPAP con casco per 10-25 minuti 4 volte al giorno, - Trattamento domiciliare con cPAP, - Terapia domiciliare con ossigeno, - Diagnosi di diabete mellito, - Infarto miocardico acuto durante i 6 mesi precedenti, - Patologie oncologiche in corso, - Insufficienza renale, - Diagnosi di tromboembolismo venoso, - BMI maggiore di 40, - Presenza di sanguinamenti incontrollati, - incapacità a comprendere o a firmare il consenso informato. |
Number of arms
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
2 |
Funding
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
ASST FATEBENEFRATELLI SACCO |
Inclusion age min
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
18 |
Inclusion age max
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
100 |
Countries
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Italy |
Type of patients
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Severe disease at enrollment |
Severity scale
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
6: Severe disease at enrollment |
Total sample size
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
160 |
primary outcome
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
The primary endpoint is the number of days of cPAP use in COVID-19 patients undergoing non-invasive cPAP helmet ventilation who neither die nor undergo mechanical ventilation. L'endpoint primario corrisponde al numero di ore di cPAP in pazienti sottoposti a ventilazione non-invasiva con casco, nei pazienti che non vanno incontro a intubazione tracheale o a morte. |
Notes
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Declared number of arm (3.0) differs from found arms (2.0) |
Phase
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
Phase 2/Phase 3 |
Arms
Last imported at : Feb. 28, 2022, 8:29 p.m. Source : EU Clinical Trials Register |
[{"arm_notes": "", "treatment_id": 873, "treatment_name": "Nebulised unfractionated heparin (ufh)", "treatment_type": "Coagulation modifiers", "pharmacological_treatment": "Pharmacological treatment"}, {"arm_notes": "", "treatment_id": 2187, "treatment_name": "Placebo", "treatment_type": "Placebo", "pharmacological_treatment": "Placebo"}] |