Clinical Trials Directory

Trials / Completed

CompletedNCT01614041

Tandospirone Citrate in the Treatment of Patients With Generalized Anxiety Disorder

Tandospirone Citrate in the Treatment of Patients With Generalized Anxiety Disorder: a Multi-center, Randomized, Usual Dose-controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
274 (actual)
Sponsor
Sumitomo Pharma (Suzhou) Co., Ltd. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy and safety of comparative high dose Tandospirone Citrate in the treatment of patients with generalized anxiety disorder.

Conditions

Interventions

TypeNameDescription
DRUGUsual dose treatment of TandospironeUsual dose treatment of Tandospirone, oral, 30 mg/day
DRUGComparative high dose of tandospirone treatmentComparative high dose of tandospirone treatment, oral, 60 mg/day

Timeline

Start date
2012-01-10
Primary completion
2018-09-11
Completion
2019-07-01
First posted
2012-06-07
Last updated
2020-01-07

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01614041. Inclusion in this directory is not an endorsement.