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
| Type | Name | Description |
|---|---|---|
| DRUG | Usual dose treatment of Tandospirone | Usual dose treatment of Tandospirone, oral, 30 mg/day |
| DRUG | Comparative high dose of tandospirone treatment | Comparative 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.