In your search for answers to unexplained infertility or recurrent pregnancy loss, we are glad you found us. While we may not be the answer for everyone, we have proven to be the solution for hundreds and hundreds of women who have all but given up hope. Our website, receptivadx.com provides details on everything you need to know about the test, how to get it, the treatments, and testimonials. Below is a quick summary.

What is ReceptivaDx?

ReceptivaDxTM is a first of its kind test for the detection of inflammation of the uterine lining most commonly associated with endometriosis, a leading cause of infertility and implantation failure. For many women, endometriosis is silent and asymptomatic.

Women testing positive for ReceptivaDx are 5 times less likely to succeed in IVF than women testing negative. ­If endometriosis is suspected it can be treated by your physician. Current treatments include hormone therapy or laparoscopy. Patients can then resume IVF attempts shortly after with renewed confidence.

While other tests evaluate the quality of embryos or determine optimal embryo transfer windows, only ReceptivaDx™ can accurately detect inflammatory conditions on the uterine lining likely to cause implantation issues.

More Information

For more information, click here to download our patient brochure.

Interested in the test? You can secure your $75 discount today. By providing your name and email, we will keep your information on file and apply your discount at the time we receive a test requisition from your doctor. All information is kept strictly confidential is never shared without permission.




    Phone: (800) 795-5385

    Email: info@cicerodx.com

    Instagram: @receptivadx (send us a direct message)

    The ReceptivaDxTM Test was developed by CiceroDx in conjunction with Pathology Consultants, Inc. of Greenville, SC. Pathology Consultants, Inc. is a laboratory certified under the Clinical Laboratory Improvement Amendments (CLIA). As with other laboratory-developed tests, this testing service has not been cleared or approved by the US FDA or any other federal regulatory agencies. Data have not been submitted to or evaluated by Federal regulatory agencies and the test is not for sale as an In Vitro Diagnostic (IVD) in the US or the EU.

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