Viewing Study NCT01259102

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Study NCT ID: NCT01259102

Status: COMPLETED

Last Update Posted: 2012-09-03

First Post: 2010-12-10

Is Gene Therapy: True

Has Adverse Events: True

Brief Title: Examine Plasma Concentrations of Buprenorphine Following Reapplication of Buprenorphine Transdermal System (BTDS) After Variable Application Site Rest Periods

Sponsor: Purdue Pharma LP

Organization:

Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Study Modules

Identification Module Status Module Sponsor Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms Interventions Module Outcomes Module Eligibility Module Contacts Locations Module Adverse Events Module Baseline Characteristics Module Participant Flow Module