IRL Grey- B 12/28/2016 RESEARCH PROTOCOL Incomplete Response in Late Life Depression: Getting to Remission with Buprenorphine Principal Investigator: Eric J. Lenze, MD Professor of Psychiatry Washington University School of Medicine Department of Psychiatry 660 S. Euclid Ave., Campus Box 8134 St. Louis, MO 63110 Voice: (314) 362-1671 E-mail:
[email protected] Collaborator: Evan Kharasch, MD Vice Chancellor for Research Russell D. and Mary B. Shelden Professor of Anesthesiology Director, Division of Clinical and Translational Research Department of Anesthesiology Professor of Biochemistry and Molecular Biophysics Washington University in St. Louis 660 S Euclid Ave, Campus Box 8054 St. Louis, MO 63110-1093
[email protected] T 314-362-8796 F 314-362-8334 Pilar Cristancho, MD Assistant Professor of Psychiatry 660 S. Euclid Ave., Campus Box 8134 St. Louis, MO 63110
[email protected] 314-362-2413 Study Team Members: Julia Schweiger, CCRC – Project Manager, Psychiatry (314) 362-3153 Marissa Rhea, MA, Clinical Research Coordinator, Psychiatry (314)-362-3797 Washington University Human Research Protection Office Washington University in St. Louis 660 S. Euclid Ave., Campus Box 8089 St. Louis, MO 63110 Sponsor: National Institute of Mental Health 1 Protocol Version 6 IRL Grey- B 12/28/2016 1. Synopsis: Study Title Incomplete Response in Late Life Depression: Getting to Remission with Buprenorphine Objective 1) To test the efficacy of buprenorphine (BPN), 2) to examine safety and tolerability of buprenorphine (BPN). Study Period Planned enrollment duration: Approximately 3 years Planned study duration: Approximately 28 to 32 weeks per subject Number of Enroll approximately 100 participants, aged 50 and older, of both sexes and Patients all races Study Medication Subjects will receive an approximate 12 week course of open-label Administration venlafaxine XR.