The effect of Prucalopride (Resolor) on gastric motor function and gastric sensitivity

TARGID0 个研究点目标入组 17 人开始时间: 2013年8月20日最近更新: 2021年3月17日

适应症

试验速览

暂无简介。

•Volunteers can participate in this study if:
•They are between 18-60 years old
•Male and female
•Patients must provide witnessed written informed consent prior to any study procedures being performed
•Are the trial subjects under 18? no
•Number of subjects for this age range:
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range 20
•F.1.3 Elderly (>=65 years) no
•F.1.3.1 Number of subjects for this age range

•Volunteers cannot participate in this study if:
•They are older than 60 years old.
•Have severely decreased kidney function.
•Have severely decreased liver function.
•Have severe heart disease, for example a history of irregular heartbeats, angina or heart attack.
•Have severe lung disease.
•Have severe psychiatric illness or neurological illness.
•Have any gastrointestinal disease
•Women that are pregnant or breastfeeding.
•Have a rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption (Resolor tablets contain lactose).

发起方

TARGID