Geneva, July 20 -- International Clinical Trials Registry received information related to the study (ChiCTR2600127834) titled 'Bioequivalence test of trazodone sustained-release tablets' on July 8.
Study Type: Interventional study
Study Design:
Cross-over
Primary Sponsor: The Affiliated Panyu Central Hospital, Guangzhou Medical University
Condition:
For depression with or without anxiety symptoms
Intervention:
Fasting T-R Group:After an overnight fast, subjects received a single oral dose of 1 tablet (150 mg) of the test formulation (T), swallowed whole with approximately 240 mL of warm water. Seven days later, after an overnight fast, subjects received a single oral dose of 1 tablet (150 mg) of the reference formulation (R, TRITT...