NIPH Clinical Trials Search

JAPANESE
UMIN ID: UMIN000005835

Registered date:01/08/2011

Comparison of potentiation of gastric mucus secretion between ranitidine and lafutidine-randamized cross-over trial

Basic Information

Recruitment status Complete: follow-up continuing
Health condition(s) or Problem(s) studiedhealthy volunteers
Date of first enrollment2011/06/01
Target sample size16
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)lafutidine ranitidine

Outcome(s)

Primary Outcomegastric mucus secretion
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximumNot applicable
GenderMale and Female
Include criteriahealthy volunteers
Exclude criteriaSystematic disease

Related Information

Contact

public contact
Name
Address 1-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi Japan
Telephone
E-mail
Affiliation Tohoku University Hospital Division of Gastroenterology
scientific contact
Name Iijima Katsunori
Address 1-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi Japan
Telephone
E-mail
Affiliation Tohoku University Hospital Division of Gastroenterology