Effect of TU-100 on Gastrointestinal and Colonic Transit in Humans

Tsumura

Status and phase

Completed

Phase 2

Phase 1

Conditions

Postoperative Ileus

Treatments

Drug: Daikenchuto (TU-100)

Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT00871325

TU100CPT1

Details and patient eligibility

About

The purpose of this study is to compare the dose related effects of orally administered TU-100, a botanical agent that modulates gastrointestinal nerves, on gastrointestinal motility and colonic transit of solids.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Subject is willing and able to provide written informed consent
Males and non-pregnant, non-breastfeeding females;
Subject is willing to undergo multiple radionuclide scans
Subject BMI is between 18 and 35 kg/m2
Subject has a negative urine drug screen
Subject has screening laboratory values that are within normal range for the analyzing laboratory

Exclusion criteria

Structural or metabolic diseases/conditions that affect the gastrointestinal system, or functional gastrointestinal disorders.
Unable to withdraw medications 48 hours prior to the study:
Alter GI transit including laxatives, magnesium or aluminum-containing antacids, prokinetics, erythromycin, narcotics, anticholinergics, tricyclic antidepressants, SSRI and newer antidepressants.
Analgesic drugs including opiates, NSAID, COX 2 inhibitors
GABAergic agents
Benzodiazepines

NOTE: Low stable doses of thyroid replacement, estrogen replacement, low dose aspirin for cardioprotection and birth control pills or depot injections are permissible.

Female subjects who are pregnant or breast feeding.
Clinical evidence (including physical exam, hemoglobin level and review of the medical history) of significant cardiovascular, respiratory, renal, hepatic, pulmonary, gastrointestinal, hematological, neurological, psychiatric, or other disease that interfere with the objectives of the study.
History of allergic reactions to ginseng, ginger, and Sichuan pepper.
History of lactose intolerance.
Subjects who are considered by the investigator to be alcoholics not in remission or known substance abusers.
Subjects who have participated in another clinical study within the past 30 days.