NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000014861

Registered date:15/08/2014

The utility and safety of intraperitoneal administration by microbubble agents for cirrhosis with refractory ascites

Basic Information

Recruitment status Open public recruiting
Health condition(s) or Problem(s) studiedCirrhosis with refractory ascites
Date of first enrollment2014/08/15
Target sample size20
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Contrast-enhanced ultrasound

Outcome(s)

Primary OutcomeThe safety of intraperitoneal administration by microbubble contrast agents
Secondary OutcomeTransit time to circulation of blood from the time of intraperitoneal administration by microbubble contrast agents

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximumNot applicable
GenderMale and Female
Include criteriaCirrotic patients with refractory ascites
Exclude criteria・Child-Pugh grade C ・Egg allergy ・Spontaneous bacterial peritonitis

Related Information

Contact

public contact
Name Tadashi Sekimoto
Address 1-8-1, Inohana, Chuou-ku, Chiba, Japan Japan
Telephone 043-226-2083
E-mail tad_sekimoto@chiba-u.jp
Affiliation Chiba University Graduate School of Medicine Department of Gastroenterology and Nephrology
scientific contact
Name Hitoshi Maruyama
Address 1-8-1, Inohana, Chuou-ku, Chiba, Japan Japan
Telephone 043-226-2083
E-mail maru-cib@umin.ac.jp
Affiliation Chiba University Graduate School of Medicine Department of Gastroenterology and Nephrology