Clinical trial

Study Evaluating Estradiol/Trimegestone in Vasomotor Symptoms (VMS) in…

NCT00195455 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Completed

Key facts

NCT number NCT00195455
Title Study Evaluating Estradiol/Trimegestone in Vasomotor Symptoms (VMS) in Post-Menopausal Women.
Official title A Prospective Open Label Study to Evaluate Vasomotor Symptoms Control and Bleeding Patterns With a Continuous Regimen of a New Progestin Trimegestone 0.125 mg and 17 b Estradiol 1 mg (Totelle),as HT on Postmenopausal Women
Lead sponsor Wyeth is now a wholly owned subsidiary of Pfizer, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Postmenopause
Intervention type Drug
Interventions Trimegestone, 17b Estradiol
Enrollment 133
Start date Feb 1, 2005
Completion Mar 1, 2007
First posted Sep 19, 2005
Last update posted Dec 20, 2007
Countries Mexico

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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