NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000015686

Registered date:13/11/2014

A clinical multicenter study on efficacy and safety of C1-inhibitor concentrate for clinical amniotic fluid embolism

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedClinical amniotic fluid embolism
Date of first enrollment2014/11/14
Target sample size30
Countries of recruitmentJapan
Study typeObservational
Intervention(s)

Outcome(s)

Primary OutcomeImprovement of clinical symptom and laboratory data
Secondary OutcomePresence or absence of side effects

Key inclusion & exclusion criteria

Age minimum16years-old
Age maximumNot applicable
GenderFemale
Include criteria
Exclude criteriaPatients with anaphylactic reaction to C1-inhibitor concentrate.

Related Information

Contact

public contact
Name Naoaki Tamura
Address 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka, Japan Japan
Telephone 053-435-2309
E-mail ntamura@hama-med.ac.jp
Affiliation Hamamatsu University School of Medicine Obstetrics and Gynecology
scientific contact
Name Naohiro Kanayama
Address 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka, Japan Japan
Telephone 053-435-2309
E-mail kanayama@hama-med.ac.jp
Affiliation Hamamatsu University School of Medicine Obstetrics and Gynecology