Join The Bloom Registry
Are you pregnant? Do you have endometriosis or uterine fibroids and/or have you taken ORILISSA® (elagolix) or ORIAHNN® (elagolix, estradiol, and norethindrone acetate capsules; elagolix capsules) prescribed by your doctor? If so, you may be able to take part in our pregnancy registry. Sharing your experience could help others with endometriosis and uterine fibroids during pregnancy.
Important Safety Information
Do not take ORILISSA® or ORIAHNN® if you are pregnant or trying to become pregnant as it may increase the risk of early pregnancy loss. If you think you may be pregnant, stop taking the medication right away and call your healthcare provider.
ORILISSA® and ORIAHNN® can change the menstrual cycle and make it hard for women to know if they are pregnant. Women taking either medication should watch for other signs of pregnancy such as breast tenderness, weight gain, and nausea.
Fill Out the Form Below to Apply
Pregnant women are often excluded from medical trials, so in order to gather information about the effects of certain medications on pregnancy, participants are needed to share their experiences after medication exposure.
What Will I Have to Do?
Fill Out Our Form
To see if you are a good fit, fill out the pre-screener form above to apply. If you qualify, someone from the team will be in touch to go over further details.
speak to the team
A registry team member will contact you to provide additional information, answer any questions you may have and complete the registration process.
Once registration is complete, you can begin answering surveys about your health currently, and in the following months through pregnancy and delivery.
Frequently asked questions
The BLOOM Pregnancy Registry has been set up to collect information from pregnant women who have taken ORILISSA® or ORIAHNN® during pregnancy, and/or who have endometriosis or uterine fibroids. By sharing your experience, you could help doctors to better understand the effects of these medications on pregnancies and babies.
If you join this registry, your involvement will last for the duration of your pregnancy and until your baby is at least 12 months old. You can expect to have study check ins once per trimester, and three times after giving birth up to 52 weeks.
Your participation in this registry is voluntary. If you decide you no longer want to participate, please contact us on the registry’s toll-free number 1-(833)-782-7241.
Although it is a good idea to notify your healthcare provider about your participation in the registry, their permission is not required. As part of your agreement to be in the study, you will give your and your baby’s healthcare providers permission to share information about you and your baby.