The primary objective of the study is to evaluate how patients with gastroparesis interpret
the instructions, item content, and response options of a daily diary questionnaire designed
to assess the key symptoms of gastroparesis.
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Locations near you
Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Full eligibility criteria for NCT01316484
Ages eligible for Study
18 Years to 70 Years
Genders eligible for Study
Accepts Healthy Volunteers
Subject has Type 1 or Type 2 diabetes mellitus
Subject is 18 to 70 years old
Subject has chronic, active symptoms of gastroparesis for at least the past three months
Subject has confirmed delayed gastric emptying by scintigraphy, a breath test, or the SmartPill® wireless motility capsule
Subject can speak and read English
Subject is able to give his/her informed consent
Subject has a cognitive, psychological or other (e.g., visual) impairment that would interfere with completing the study visit
All locations for NCT01316484
United States (4)
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Wake Forest University Health Sciences
Winston-Salem, North Carolina, United States, 27517
Temple University Health Sciences Center
Philadelphia, Pennsylvania, United States, 19140
Texas Tech University Health Sciences Center
El Paso, Texas, United States, 79905
View full eligibility
Tris trial is registered with FDA with number: NCT01316484. The sponsor of the trial is Tranzyme, Inc. and it is looking for 40 volunteers for the current phase.
Official trial title: Protocol for the Patient Understanding (Cognitive Debriefing) of a Modified Gastroparesis Cardinal Symptom Index (GCSI) Daily Diary
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