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Study to Examine the Effect of Gastric Bypass Surgery on Venlafaxine ER Blood Levels

Bariatric Surgery Clinical Trial

Official title:
Pharmacokinetic Study Comparing Area Under the Curve for a Single Dose of Venlafaxine ER Pre- and Post-gastric Bypass

Clinical Trial Summary

The purpose of the study is to determine whether a significant and predictable change in bioavailability of extended-release venlafaxine occurs following Roux-en-Y gastric bypass.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01867255
Study type Interventional
Source Mayo Clinic
Contact
Status Completed
Phase Phase 1
Start date October 2013
Completion date March 2015
View Details
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