Clinical Trials Directory

Trials / Completed

CompletedNCT01149369

Aprepitant for the Relief of Nausea in Patients With Chronic Nausea and Vomiting of Presumed Gastric Origin Trial

Aprepitant for the Relief of Nausea in Patients With Chronic Nausea and Vomiting of Presumed Gastric Origin: A Multicenter, Randomized, Double-Masked, Placebo-Controlled Trial

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
126 (actual)
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) · NIH
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The principal objective of this multicenter, randomized, placebo-controlled trial is to evaluate whether 4 weeks of treatment with aprepitant will improve nausea as compared with placebo in patients with symptoms of chronic nausea and vomiting of presumed gastric origin.

Detailed description

APRON is a multicenter, randomized, double-masked, placebo controlled trial of 4 weeks of treatment with aprepitant or placebo for patients with symptoms of gastroparesis and related disorders. Screening for eligibility and collection of baseline data will span up to 4 weeks after obtaining informed consent and registration. Eligible patients will consist of patients with symptoms of gastroparesis and will be randomized to either aprepitant (125 mg per day) or placebo for 4 weeks. The symptoms will be measured with the Gastroparesis Cardinal Symptom Index Daily Diary (GCSIDD) for one week at baseline and for four weeks after randomization. In addition, the nausea symptom will be measured daily on a 0 to 100 mm visual analog scale (VAS) for one week at baseline and daily for four weeks after randomization. There will be a 2 week washout period at the end of the treatment to ensure patient safety following the end of treatment.

Conditions

Interventions

TypeNameDescription
DRUGAprepitantAprepitant, 125 mg, 1 capsule, q.d. (everyday) with lunch for 4 weeks
DRUGPlaceboAprepitant-placebo, 125 mg, 1 capsule, q.d. (everyday) with lunch for 4 weeks

Timeline

Start date
2013-04-01
Primary completion
2015-08-01
Completion
2015-09-01
First posted
2010-06-23
Last updated
2019-05-08
Results posted
2019-05-08

Locations

8 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01149369. Inclusion in this directory is not an endorsement.