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Vitrification Versus Slow Freezing of Human Day 3 Embryos

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified January 2008 by University Hospital, Gasthuisberg.
Recruitment status was:  Active, not recruiting
Information provided by:
University Hospital, Gasthuisberg Identifier:
First received: January 4, 2008
Last updated: July 3, 2008
Last verified: January 2008
In assisted reproduction technology (ART), cryopreservation of embryos maximizes the potential of IVF cycles. Currently different cryopreservation methods are used, the conventional slow freezing method and vitrification. There is, therefore an immediate need to assess which cryopreservation technique is preferential in human IVF. In this prospective randomised study conventional slow freezing and vitrification, using the Hemi-straw carrier system, of human day 3 embryos were compared.

Condition Intervention
Cleavage Stage, Ovum Procedure: vitrification

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Vitrification Versus Slow Freezing of Human Day 3 Embryos

Further study details as provided by University Hospital, Gasthuisberg:

Primary Outcome Measures:
  • Pregnancy rate [ Time Frame: 9 months ]

Secondary Outcome Measures:
  • survival rate after thawing of embryos [ Time Frame: 24 hours ]

Enrollment: 901
Study Start Date: October 2005
Estimated Study Completion Date: December 2008
Arms Assigned Interventions
Experimental: 1
Procedure: vitrification
Vitrification using Hemi-straw carrier system.
No Intervention: 2
Slow freezing

  Show Detailed Description


Ages Eligible for Study:   18 Years to 43 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Embryos of sufficient embryo quality: at least 6 cells on day 3 and less than 20 % fragmentation.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00710723

UZ Leuven
Leuven, Belgium, 3000
Sponsors and Collaborators
University Hospital, Gasthuisberg
Principal Investigator: D'Hooghe Thomas, Prof. Dr. UZ Leuven
  More Information

Responsible Party: Prof. Dr. Thomas D'Hooghe, University Hospital, Gasthuisberg. Identifier: NCT00710723     History of Changes
Other Study ID Numbers: dwille1
Study First Received: January 4, 2008
Last Updated: July 3, 2008 processed this record on August 22, 2017