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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02852356
Other study ID # 2016-TiMMI-001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2016
Est. completion date December 22, 2017

Study information

Verified date April 2024
Source Ovation Fertility
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of the MIRI-TL time-lapse incubator and CultureCoin dish compared to standard big-box incubators and standard culture dishes used for embryo culture.


Description:

Following randomization and standard ovarian stimulation protocols to obtain a sufficient number of mature (MII) oocytes, these oocytes will be fertilized by Intra-Cytoplasmic Sperm Injection (ICSI). If a patient has been randomized to the study group, all inseminated oocytes and subsequently all fertilized diploid (2PN) zygotes will be placed in the CultureCoin and then into the MIRI-TL Time-lapse incubator and cultured as per normal protocol to the blastocyst stage (Day 5/6 or 7). Top quality blastocyst(s) will be transferred and monitored for implantation, pregnancy and ongoing birth. Embryo transfers will either occur in a fresh or frozen embryo transfer cycle.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date December 22, 2017
Est. primary completion date December 22, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - At least 18 years of age - Women undergoing in vitro fertilization treatment using their own or frozen oocytes - Fresh or Frozen Embryo Transfer - Fertilization by ICSI - At least 4 diploid (2PN) embryos at fertilization check - Willing to have all inseminated oocytes imaged by Miri - Willing to comply with study protocol and procedures Willing to provide written informed consent Exclusion Criteria: - Fertilization using surgically removed sperm - History of cancer

Study Design


Related Conditions & MeSH terms


Intervention

Device:
MIRI-TL Incubator
MIRI-TL Timelapse incubator

Locations

Country Name City State
United States Ovation Fertility Austin Texas

Sponsors (1)

Lead Sponsor Collaborator
Ovation Fertility

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants With a Positive bHCG Level as Detected by a Blood Test Human Chorionic Gonadotropin (hormone made by cells formed in the placenta) are detected by a blood test. An hCG level >50mIU/mL is considered to be a successful pregnancy. 14 days after embryo transfer
Secondary Number of Patients With Embryo Implantation Presence of Gestational Sac by ultrasound indicates a positive pregnancy. 28 days
Secondary Embryo Development Blastocyst Utilisation Rate (number of fertilised embryos which develop to usable blastocysts) 7 days
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