Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:52 AM
Ignite Modification Date:
2025-12-25 @ 2:52 AM
NCT ID:
NCT04447833
Eligibility Criteria:
Inclusion Criteria:
* Willing and able to provide written informed consent prior to performing study procedures (and have given written consent)
* Coronavirus (SARS-CoV-2) infection confirmed by polymerase chain reaction (PCR) test at screening
* Male or female patient aged 18 to 65 years old
* Patient must fulfil the Berlin Definition of severe ARDS within 3 weeks to 48 hours prior to enrolment (Will be assessed once the patient has been admitted to the ICU)
* Patient is on respirator support within 3 weeks to 48 hours prior to enrolment (Will be assessed once the patient has been admitted to the ICU)
* Pregnancy test in blood confirming negative results before enrolment (for women ≤55 years old)
Exclusion Criteria:
* History of any clinically significant disease or disorder which, in the opinion of the Investigator, may either put the patient at risk because of participation in the study, or influence the results or the patient's ability to participate in the study
* Patients with history of treated blood and/or solid organ malignancy with recurrence within five years prior to dosing of the ATIMP are to be excluded. Patients with history of cervix cancer and non-melanoma skin cancer with recurrence within two years prior to dosing of the ATIMP are to be excluded
* Pregnant or breast feeding female
* Patient with a history of anti-coagulation therapy for other indications that short-term prophylaxis after surgery
* Patients with a history and/ or on-going treatment for entity associated with bleeding disorder or potential risk for bleeding (e.g. inflammatory bowel disease, gastro-esophagitis with or without ulcers, haemophilia and other bleeding disorders, inflammatory musculo-skeletal disease with potential bleeding complications)
* Patients with a history during the latest five years and/or on-going treatment for systemic infection (e.g. Septicaemia due to in vivo foreign body (e.g. stents, catheters, heart valve), tuberculosis, malaria, other opportunistic and parasite infections)
* Prisoner
* Any other irreversible disease or condition for which six-month mortality is estimated to be greater than 50%
* Moderate to severe liver failure (Child-Pugh Score \>12)
* Reduced renal function with a creatinine clearance (Cockcroft-Gault Equation) \< 45 mL/min/1.73m2
* Severe chronic respiratory disease with a PaCO2 \>50 mmHg or the use of home oxygen
* Major trauma in the prior 5 days
* Lung transplant patient
* Patients on ECMO-support
* Patients with a previous history of severe burns
* Documented deep venous thrombosis or pulmonary embolism within past three months
* Known hypersensitivity to DMSO
* Investigator considers the patient unlikely to comply with study procedures, restrictions and requirements
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT04447833
Study Brief:
Protocol Section:
NCT04447833