Infertility Clinical Trial
— OxygenOfficial title:
A Controlled Randomized Trial Evaluating the Effect of Lowered Incubator Oxygen Tension on Live Births in a Predominantly Blastocyst Transfer Program
Verified date | June 2008 |
Source | Texas Health Resources |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The potentially damaging effect of free O2 radicals to cultured embryos may be reduced by adding scavengers to the culture media or by reducing the incubator O2 levels. However, lowering the O2 in the culture environment can be expensive, troublesome and may not be justifiable. The objective of this study is to evaluate the effect of lowered incubator O2 tension on live birth rates in a predominately day-5 embryo transfer program. The hypothesis of this study is that a lowered (more physiological)oxygen concentration in embryo culture incubators will increase live birth rates for in vitro fertilization patients. 230 first-cycle women undergoing routine IVF or ICSI with ejaculated sperm will be randomized in a prospective clinical trial and stratified for patient age and physician. Embryos of patients will be randomly assigned for culture in either a 21% O2 (atmospheric) or 5% O2 (reduced) environment. Clinical endpoints monitored will be rates of implantation, clinical pregnancy, live birth and blastocyst cryopreservation.
Status | Completed |
Enrollment | 230 |
Est. completion date | August 2001 |
Est. primary completion date | August 2001 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 40 Years |
Eligibility |
Inclusion Criteria: - First IVF cycle or donor oocyte cycle - IVF or ICSI - Ejaculated sperm only for ICSI - <41 years of age Exclusion Criteria: - One or more failed IVF cycles - 40 years of age - Using testicular or epididymal sperm for fertilization |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Presbyterian Hospital of Palno | Plano | Texas |
Lead Sponsor | Collaborator |
---|---|
Texas Health Resources |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Live birth | 9 months | No | |
Secondary | Implantation rate | 6 weeks | No |
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