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:
2025-12-24 @ 7:22 PM
Ignite Modification Date:
2025-12-24 @ 7:22 PM
NCT ID:
NCT00771303
Eligibility Criteria:
Inclusion Criteria:
* All pregnant patients with a clinical suspicion of acute PE will be included in the study, provided they correspond to the following diagnostic and exclusion criteria, and they have signed an informed consent form.
Exclusion Criteria:
* Age less than 18 years
* Absence of informed consent
* Patients allergic to contrast medium
* Impaired renal function (creatine clearance less than 30 ml/min as estimated by the Cockroft formula)
* Geographic inaccessibility for follow-up
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT00771303
Study Brief:
Protocol Section:
NCT00771303