Recurrent Pregnancy Loss
Conditions
Brief summary
The trial will conclude after the inclusion and follow-up (pregnancy loss or 6 months after live birth) for 186 women. Included women who become pregnant less than two months after starting the medication or do not achieve pregnancy within one year of starting the medication will be replaced 1:1 by new patients included in the trial.
Interventions
Sponsors
Hvidovre Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 64 Years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The trial will conclude after the inclusion and follow-up (pregnancy loss or 6 months after live birth) for 186 women. Included women who become pregnant less than two months after starting the medication or do not achieve pregnancy within one year of starting the medication will be replaced 1:1 by new patients included in the trial. | — |
Countries
Denmark
Outcome results
None listed