CompletedPhase 2NCT04135417
Safety and Efficacy Assessment of HAV in Patients Needing Vascular Access for Dialysis
Studying Complication in hemodialysis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Humacyte, Inc.
- Principal Investigator
- Shamik Shamik, MD, M.DHumacyte, Inc.
- Intervention
- HAV(biological)
- Enrollment
- 30 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2022
Study locations (2)
- Szpital Kliniczny Przemienienia Pańskiego UM w Poznaniu, Klinika Chirurgii Ogólnej i Naczyń, Poznan, Poland
- Wojewódzki Szpital Specjalistyczny we Wrocławiu, Oddział Chirurgii Naczyniowej, Wroclaw, Poland
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT04135417 on ClinicalTrials.govOther trials for Complication in hemodialysis
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