Clinical Investigation to Evaluate the Hemanext® Oxygen Reduction System - Pivotal Trial
Summary
The registered summary isn't in our current data snapshot. Read it on the ClinicalTrials.gov record ↗. Why? →
Investigators
The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.
- Faye West, MD
American Red Cross Mid-Atlantic Research Facility
Principal Investigator - Jose A Cancelas Perez, MD, PhD
Hoxworth Blood Center
Principal Investigator - Matthew Karafin, MD
Versiti Blood Health
Principal Investigator
A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.
Sites
3 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.
- Hoxworth Blood Center, University of Cincinnati
Cincinnati, Ohio, United States
- American Red Cross Mid-Atlantic Research Facility
Norfolk, Virginia, United States
- Blood Center of Wisconsin
Milwaukee, Wisconsin, United States
Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.
Drugs studied
No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →
Registration & key dates
Registry attributes as recorded on the ClinicalTrials.gov study record.
- Start
- 27 Nov 2017
- Primary completion
- 6 Mar 2019
- Completion
- 6 Mar 2019
- Last update posted
- 23 Jun 2020
- Registered enrollment
- 100
- Registry id
- NCT03301779
Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 12 Jul 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.