Luteal phase insufficiency in assisted reproduction Pregnancy and Childbirth Luteal phase insufficiency
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Women 2. Aged between 28 and 39 years, 3. Failed to become pregnant 4. Had low luteal-phase progesterone levels in a previous in vitro fertilization attempt
Exclusion criteria
Exclusion criteria: 1. Age of >40 years 2. Andrological gynecological and systemic pathologies unrelated to the corpus luteum function: 2.1. Azoospermia 2.2. Necrozoospermia 2.3. Uterine polyps and fibroids 2.4. Polycystic ovary syndrome 2.5. Endometriosis 2.6. Cushing syndrome 2.7. Diabetes 2.8. Hypothyreosis and hyperthyreosis 2.9. Body mass index >29
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical pregnancy rate (number of pregnancies divided by the number of embryo transfer procedures) is measured from medical records 3 months after embryo transfer | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Implantation rate (number of gestational sacs containing a living embryo implanted in the uterus divided by the number of embryos transferred) is measured from medical records 6 weeks after embryo transfer 2. Serum progesterone concentration is measured using immunoassay at the 7th and 14th day after embryo transfer 3. Total dose of progesterone administered is measured from medical records at the 14th day after embryo transfer | — |
Countries
Spain