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Biopsies should be collected in the luteal phase of a natural cycle 7-10 days after ovulation is detected. In Mock cycles, biopsies should be collected 5-10 days after the start of progesterone.

The sample is then sent to either our South Carolina, Bellingham Washington, or New Jersey laboratories. Results are available 7-10 days after arrival in our testing facility. Cicero Diagnostics provides collection kits at no-charge to our customers.

In the event a sample is collected without one of our kits available, please place the endometrial biopsy in a vial containing 10% formalin and contact us to arrange for shipment.​ A test request form is included with every collection kit. For additional Test Request Forms, Please call Customer Service at 800-795-5385.

Is Biopsy date dependent on Cycle?

Yes:

Define the ReceptivaDx Biopsy Date Range based on the Natural or Mock Cycle info below.

Natural Cycle:

  • 7-10 days after ovulation occurs

Mock Cycle:

  • 5-10 days after start of progesterone

 

Once collected, the sample is placed in a preservative (10% formalin vial) and is sent overnight via FedEx to our testing facility. Samples remain stable once placed in formalin. Samples can be shipped Monday through Friday. Results are available typically within 7-10 days.

Who is a candidate for ReceptivaDx testing?

Candidates include:

  • All women with unexplained infertility
  • Women who have failed one or more IVF cycles
  • Women who have experienced recurrent pregnancy loss
  • Women who cannot afford IVF or that have limited fertility coverage

The ReceptivaDxTM Test was developed by Cicero Diagnostics 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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