Clinical trial
Lexapro in the Treatment of Patients With Postpartum Depression
NCT00277108 · University of Rochester, Other · Completed
Key facts
| NCT number | NCT00277108 |
|---|---|
| Title | Lexapro in the Treatment of Patients With Postpartum Depression |
| Official title | Open Label Variable Dose Escitalopram (Lexapro) in the Treatment of Patients With Postpartum Major Depression: A Pilot Study |
| Lead sponsor | University of Rochester, Other |
| Collaborators | Forest Laboratories Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Postpartum Depression |
| Intervention type | Drug |
| Interventions | Escitalopram (Lexapro) |
| Enrollment | 20 |
| Start date | Feb 1, 2004 |
| Primary completion | Apr 1, 2007 |
| Completion | Apr 1, 2007 |
| First posted | Jan 13, 2006 |
| Last update posted | Nov 6, 2008 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About ClinicalTrials.gov studies
ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.
Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: