Prospective, Randomised, Double-blind, Placebo Controlled, Phase III Clinical Study Assessing the Efficacy of 25 mg Natural Progesterone Administered Subcutaneously in Restoring the Normal Luteal Phase in Women With Previous Diagnosis of Luteal Phase Deficiency

Trial Profile

Prospective, Randomised, Double-blind, Placebo Controlled, Phase III Clinical Study Assessing the Efficacy of 25 mg Natural Progesterone Administered Subcutaneously in Restoring the Normal Luteal Phase in Women With Previous Diagnosis of Luteal Phase Deficiency

Not yet recruiting
Phase of Trial: Phase III

Latest Information Update: 14 Jul 2017

At a glance

  • Drugs Progesterone (Primary)
  • Indications Female infertility
  • Focus Registrational; Therapeutic Use
  • Sponsors IBSA
  • Most Recent Events

    • 07 Jul 2017 Planned initiation date changed from 1 Mar 2017 to 1 Sep 2017.
    • 10 Nov 2016 New trial record
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