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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03184519
Other study ID # 1701-VLC-011-EB
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 19, 2017
Est. completion date August 10, 2018

Study information

Verified date July 2020
Source Instituto Valenciano de Infertilidad, IVI VALENCIA
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Proof of concept study for the prediction of ongoing pregnancy in women undergoing In-Vitro Fertilization (IVF), using hyperglycosylated human chorionic gonadotropin (hhCG), early after In-Vitro Fertilization and fresh Embryo Transfer (IVF-ET).


Recruitment information / eligibility

Status Completed
Enrollment 156
Est. completion date August 10, 2018
Est. primary completion date August 10, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion criteria:

- Written informed consent

- Patients undergoing their first or second IVF-ET cycle

- Age 18-45 years

- Use of Ovitrelle for final follicular maturation and luteinization

- Fresh or Frozen day-5 blastocysts transrer (Autologus or Egg donation)

Exclusion criteria:

- Gestational surrogacy (patient's eggs used for pregnancy in a surrogate mother)

- Canceled IVF cycles

- GnRH agonist triggering cycles in the case of fresh ET.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Pregnancy test
Instead of one blood sample, patients will have three blood analyses to predict pregnancy earlier after the embryo transfer.

Locations

Country Name City State
Spain IVI Valencia Valencia

Sponsors (1)

Lead Sponsor Collaborator
Instituto Valenciano de Infertilidad, IVI VALENCIA

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants With Early Detection of Pregnancy Detection of Pregnancy on earlier dates (before day-11 after Embrio transfer) One month