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NCT00126022 · ClinicalTrials.gov registry record · Phase 3
Intravenous Tedisamil in the Rapid Conversion of Atrial Fibrillation or Flutter to Normal Sinus Rhythm in Female Subjects
A Phase 3 study of Atrial Fibrillation and Atrial Flutter, sponsored by Solvay Pharmaceuticals.
- Completed
- Registry status
- Phase 3
- Development phase
- 20
- Study locations
NCT00126022: Completed Phase 3 study of Atrial Fibrillation and Atrial Flutter, sponsored by Solvay Pharmaceuticals.
NCT00126022 is a Phase 3 study of Atrial Fibrillation and Atrial Flutter that has completed, run by Solvay Pharmaceuticals. The trial reports 20 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00126022, a Phase 3 study of Atrial Fibrillation and Atrial Flutter, has completed, sponsored by Solvay Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 20
- Study locations
Study Summary
The purpose of this study is to demonstrate the ability of tedisamil to convert atrial fibrillation or flutter into normal sinus rhythm (NSR) in female patients.
Conditions Studied
Interventions
- DRUG Tedisamil sesquifumarate
Study Locations (20)
Other
- Site 2 - Buenos Aires
- Site 3 - Buenos Aires
- Site 5 - Munro
- Site 4 - San Miguel de Tucumán
- Site 8 - Brno
- Site 11 - Jindřichův Hradec
- Site 9 - Ostrava-Poruba
- Site 10 - Pilsen
- Site 14 - Prague
- Site 6 - Prague
- Site 7 - Prague
- Site 12 - Slaný
- Site 13 - Ústí nad Orlicí
- Site 15 - Bad Nauheim
- Site 17 - Göttingen
- Site 16 - Halle
- Site 18 - Haifa
- Site 19 - Jerusalem
- Site 22 - Jerusalem
Tennessee
- Site 82 - Tullahoma
Trial Details
| Field | Value |
|---|---|
| Start Date | 2004-12 |
| Est. Completion | 2006-03 |
| Phase | Phase 3 |
What the finished NCT00126022 record still lists
NCT00126022 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.
The record links to 2 conditions, with Atrial Fibrillation appearing as the primary indexed condition, and to 1 intervention - of which Tedisamil sesquifumarate is the first listed.
NCT00126022 names 20 study sites across 2 states, led by Other, Tennessee.
Frequently Asked Questions
What is clinical trial NCT00126022 about?
NCT00126022 is a clinical study titled "Intravenous Tedisamil in the Rapid Conversion of Atrial Fibrillation or Flutter to Normal Sinus Rhythm in Female Subjects". The purpose of this study is to demonstrate the ability of tedisamil to convert atrial fibrillation or flutter into normal sinus rhythm (NSR) in female patients.
What is the current status of trial NCT00126022?
This trial is currently completed. It is a Phase 3 study. The study started on 2004-12. Estimated completion is 2006-03.
What conditions does trial NCT00126022 study?
This clinical trial studies the following conditions: Atrial Fibrillation, Atrial Flutter.
What interventions are being tested in trial NCT00126022?
The interventions under investigation include: Tedisamil sesquifumarate (DRUG).
Who is sponsoring clinical trial NCT00126022?
This trial is sponsored by Solvay Pharmaceuticals, which has 35 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00126022 being conducted?
This trial has 20 study locations across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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