Comparing IVF results when using two commercially available culture media (part 2) - a multi-centre randomized controlled trial

Completed

• Conditions: subfertiliteit; fecundity; subfertility

• Registration Number: NL-OMON47201
• Lead Sponsor: Medisch Universitair Ziekenhuis Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 1980

Inclusion Criteria

All couples that present to one of the participating centres for an IVF/ICSI treatment.

Exclusion Criteria

Patients undergoing a PGD cycle, patients undergoing a modified natural cycle, patients requiring gestational surrogacy and patients who participated in the study before will be excluded.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Live birth rate</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Embryo development, implantation rate, clinical pregnancy rate, miscarriage<br /><br>rate, ongoing pregnancy rate, multiple pregnancy rate, morphometric parameters<br /><br>of foetal development at 8, 12 and 20 weeks of pregnancy, mean values of<br /><br>maternal serum markers during first trimester screening, mean birth weight,<br /><br>mean gestational age at birth and percentage of children with congenital<br /><br>abnormalities.</p><br>