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 @ 1:14 AM
Ignite Modification Date:
2025-12-25 @ 1:14 AM
NCT ID:
NCT04646993
Eligibility Criteria:
Inclusion Criteria:
1. subjects who provided a written informed consent and authorization for disclosure of protected health information;
2. male and female adult or elderly patients of any ethnicity having had a first-ever event of provoked or unprovoked DVT of the lower limbs and/or PE and treated with oral anticoagulant
3. for whom the center is in possession of all the data relevant to the index event;
4. having a permanent reference contact.
Exclusion Criteria:
1. subjects \<18 years old;
2. subjects unable or unwilling to issue the written informed consent;
3. subjects for whom the information relevant to the index event are incomplete or inaccessible to the Investigator;
4. subject in whom the index event was a DVT not of the lower limbs;
5. subjects with life expectancy of less than 2 years;
6. subjects participating in any other clinical study, regardless of its nature;
7. subjects considered, by the attending physician, unable to comply with the study procedures.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04646993
Study Brief:
Protocol Section:
NCT04646993