drugset / Trial / NCT00944268

Efficacy and Tolerability Study to Treat Mild and Moderate Anxiety

NCT00944268 ↗

Phase 3 Unknown 124 enrolled Ativus Farmaceutica Ltda
RandomizedFactorialOpen-labelTreatment

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.

Timeline

Start
2009-09
Primary completion
2009-12
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Passiflora Traditional medicine (herbal / TCM) — —

Indications