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 @ 1:47 PM
Ignite Modification Date:
2025-12-24 @ 1:47 PM
NCT ID:
NCT03770195
Eligibility Criteria:
Preoperative Inclusion Criteria:
* Patient is undergoing a primary full abdominoplasty procedure without concomitant liposuction; and
* Patient is willing and able to give written informed consent for registry participation
Preoperative Exclusion Criteria:
* Patient has a known sensitivity or allergy to bovine and/or porcine substance(s); and
* Patient has religious or other objections to porcine, bovine, or human components
Intraoperative Inclusion Criteria
* Patient has at least one Target Bleeding Site (TBS) with minimal, mild, or moderate bleeding for which conventional means for hemostasis are ineffective or impractical; and
* The surgeon elects to utilize HEMOBLAST™ Bellows per its approved Indications for Use
Sex:
ALL
Study:
NCT03770195
Study Brief:
Protocol Section:
NCT03770195