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 @ 1:40 AM
Ignite Modification Date:
2025-12-25 @ 1:40 AM
NCT ID:
NCT01793194
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women 18-45 years of age.
* Fetal gestation between 8-20 weeks.
* Patient is seeking care for the pregnancy at one of the study locations (Johns Hopkins East Baltimore Campus, Johns Hopkins Bayview Medical Center, and Johns Hopkins at White Marsh).
* Ability to complete informed consent and willingness to comply with protocol (return for all follow-up visits \& participate in phone interviews).
Exclusion Criteria:
* Inability to wear compression stockings.
* Women who currently have been prescribed to wear compression stockings by a medical professional.
* Chronic dermatological condition (i.e. psoriasis).
* Chronic deep vein thrombus or chronic phlebitis.
* In women with varicose veins: Presence of primary outcome (superficial thrombophlebitis or DVT) on first visit ultrasound.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT01793194
Study Brief:
Protocol Section:
NCT01793194