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Venlafaxine PK Following Bariatric Surgery — VLX  

Sleeve Gastrectomy Clinical Trial

Official title:
A Comparison of Immediate and Extended Release Venlafaxine Following Bariatric Surgery

Clinical Trial Summary

This study is being conducted to evaluate how the body absorbs and processes the immediate release (IR) and sustained release (XR) medication venlafaxine (Effexor®). Subject who are 1-3 years post gastric bypass or sleeve gastrectomy surgery will be invited to participate. Non-surgical controls will also be enrolled based on a matching criteria to post gastric bypass subjects. Participants will be asked to complete two 12-hour study days approximately 11 days apart. This study will enroll up to 30 participants.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02005107
Study type Interventional
Source North Dakota State University
Contact
Status Completed
Phase Phase 4
Start date December 2013
Completion date March 2015
View Details
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