Effects of Gastric Bypass on Blood Levels of Duloxetine

Status Completed

Clinical Trial Summary

This study aims to determine the difference, if any, in the pharmacokinetics of duloxetine between patients who are nine to fifteen months post Roux-en-Y Bariatric Surgery and control subjects matched for body mass index (BMI), age and gender.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Bio-availability Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science

Related Conditions & MeSH terms

Bariatric Surgery

Clinical Trial Details

NCT number	NCT00989157
Study type	Interventional
Source	Neuropsychiatric Research Institute, Fargo, North Dakota
Contact
Status	Completed
Phase	Phase 3
Start date	September 2009
Completion date	November 2012

View Details

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