ClotFoam as an Adjunct to Hemostasis in Abdominal Surgery - Liver Bleeding is Encountered
Status unconfirmed · Phase 1
Conditions studied: Bleeding
In brief
Phase 1 Single-Arm Study Evaluating ClotFoam as an Adjunct to Hemostasis in Abdominal Surgery in Which Liver Bleeding is Encountered.
Key facts
- Study ID
- NCT02264730
- Run by
- Biomedica Management Corporation
- People needed
- 20
- Starts
- 2014-07-01
- Expected to finish
- 2015-01-01
- Last updated by the study team
- 2014-10-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subject is expected to survive 6 months from the date of screening, If female and of child-bearing potential, subject has a negative serum pregnancy test prior to surgery and agrees to not breast feed her child (if applicable) for duration of study treatment and completion of study follow-up visits, If subject is a sexually active male or a sexually active female of child-bearing potential, subject agrees to use a medically accepted form of contraception from the time of consent to completion of all follow-up study visits
You may not qualify if…
- pregnant females
Where it is running
- Washington University School of Medicine Barnes Jewish Hospital Clinical Laboratory — St Louis, Missouri, United States (enrolling)
Full record on ClinicalTrials.gov
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