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 @ 6:59 PM
Ignite Modification Date:
2025-12-24 @ 6:59 PM
NCT ID:
NCT02289157
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women with BMI \> 40 undergoing a cesarean delivery at Parkland Health and Hospital System.
Exclusion Criteria:
* Any patient not meeting inclusion criteria will be deemed ineligible.
* All HIV positive patients will be excluded due to the increased risk of infectious complications in these patients.
* Although patients on anticoagulants can use NPWT, they will be excluded as there may be an increased risk of bleeding in these patients.
* according to the wound therapy manufacturer's instructions patients with:
* fragile skin
* allergy to silver or acrylic adhesives
* a malignancy in the wound bed or margins of the wound bed
* non-enteric and unexplored fistulas
* necrotic tissue with eschar present
* exposed arteries, veins, nerves or organs, anastomotic sites, or surgical suction are not candidates for usage of the device.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
10 Years
Maximum Age:
64 Years
Study:
NCT02289157
Study Brief:
Protocol Section:
NCT02289157