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Clinical Trial Summary

At the start of the controlled ovarian stimulation as a part of the IVF/ICSI treatment patients are informed about this trial. In case they gave informed consent and they have a progesterone level between 1 and 1.5 ng/ml at the day of the hCG injection, they will be randomised. One group of patients will have a fresh embryo transfer, in the second group all embryos will be cryopreserved and transfered in a subsequent (natural or artificial) cycle. The aim of this study is to compare clinical pregnancy rate between the two groups.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03162315
Study type Interventional
Source University Hospital, Ghent
Contact
Status Completed
Phase N/A
Start date March 2016
Completion date August 3, 2018

See also
  Status Clinical Trial Phase
Completed NCT03350646 - Does the Volume of the Embryo Culture Medium During Embryo Transfer Affects the IVF Outcomes? N/A
Completed NCT04175990 - IVF Outcome Following Progestogen Ovarian Stimulation Phase 1
Recruiting NCT02496754 - The Application of a New Ovarian Stimulation Protocol in IVF N/A
Recruiting NCT03006406 - Effect of Shorten Gonadotropin-releasing Hormone Agonist Therapy on the Outcome of in Vitro Fertilization-Embryo Transfer in Patients With Endometriosis N/A
Recruiting NCT06165367 - Hyaluronan-enriched Medium and Euploid Blastocyst Transfers N/A
Terminated NCT00737984 - Improving the Pregnancy Rate With Endometrial Sampling Before Intrauterine Insemination N/A