KOKO Serene Study

KOKO Serene Study

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Study Details

Full Title

Clinical Trial Designed to Assess the Safety and Effectiveness of
the KOKO™ device In Treating Primary Abnormal Postpartum Uterine
Bleeding or Hemorrhage (“PPH”)

Principal Investigator

Jerome
Federspiel

Protocol Number

PRO00118826

NCT ID

NCT06452355

Enrollment Status

Open to Enrollment