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Efficacy and Tolerability Study to Treat Mild and Moderate Anxiety — E01ATCAL0308  

Anxiety Clinical Trial

Official title:
Clinical Study Phase III, Multicenter, Prospective, Open to Evaluate the Efficacy and Tolerability of the Combination Use of Passiflora Incarnata L, Crataegus Oxyacantha and Salix Alba L in Mild and Moderate Anxiety

Clinical Trial Summary

To evaluate the efficacy and tolerability of the combination use of Passiflora incarnata L, Crataegus oxyacantha and Salix alba L in mild and moderate anxiety.

Clinical study phase III, multicenter, prospective, open.

Patients will be included in sufficient quantity to achieve the minimum number of 124 evaluable patients.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00944268
Study type Interventional
Source Ativus Farmaceutica Ltda
Contact Dagoberto Brandão
Phone 55 11 36733763
Email dagoberto@phcbrasil.com.br
Status Not yet recruiting
Phase Phase 3
Start date September 2009
Completion date January 2010
View Details
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