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Clinical study of Time-Lapse incubator

Clinical Evaluation of Time-lapse Incubator System in Blastocyst Development: Multi-centre prospective study - RCT-TLI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055611
Enrollment
400
Registered
2024-11-01
Start date
2022-08-20
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients seeking ART treatments with in vitro fertilization, embryo culture and transfer.

Interventions

Fertilized oocytes in the treatment cycles which meet the selection criteria after insemination will be randomly split into the test arm and the control arm. Embryos in the test arm are cultured in t
EmbryoScope+ time lapse incubator&quot
. Embryos are cultured continuously up to blastocysts stage, usually for 5-7 days from the insemination. Embryos in the control arm are cultured in the conventional incubator normally used in the t

Sponsors

Vitrolife K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients and treatment cycles must meet all of the following conditions: (1) Received informed consent (IC) by physician and signed the IC agreement form. The patient age must be between 20 and 50 on the day of signing the agreement. (2) Shown to be eligible to the standard IVF treatment procedure in the study clinics by the initial diagnosis results collected before starting IVF treatment. (3) Treatment cycles with six or more of oocytes fertilized normally by either cIVF or ICSI.

Exclusion criteria

Exclusion criteria: Patients or treatment cycles applicable to any one of the following conditions: (1) Fertilization is performed with sperms collected through special procedure for male infertility patients: e.g., TESA and TESE. (2) Fertilization is performed with both cIVF and ICSI in a single treatment cycle. (3) Any treatment cycles in which an embryo, either in the study arm or in the control arm, is taken out from the culture for embryo transfer before reaching to blastocysts, such as day 2/3 embryo transfer. (4) Oocytes which require in vitro maturation (IVM) shall be excluded from the sample pool. However, it shall include those treatment cycles found with six or more of normally fertilized oocytes after excluding IVM oocytes. (5) Patients already been registered in any other clinical studies.

Design outcomes

Primary

MeasureTime frame
Those rates shall be denominated by per M-II oocytes and per-2PN embryo. (1)Overall blastocyst rate, observed between day 5 and day 7 (2)Good blastocyst rate: Grade 3BB or better between day 5 and day 7 (3)Number of Usable Blastocysts per cycles: embryos meeting the criteria of fresh transfer and freezing of the study clinics

Secondary

MeasureTime frame
(1) 2PN rate after the insemination, embryo morphology grades on day 3 (2) Grade AA/AB/BA blastocysts (top-rated blastocysts) (3) ET outcomes, including HCG+/-, CPR verified by GS in week 7, OPR verified by fetal heartbeats in week 13

Countries

Japan

Contacts

Public ContactSouichi Ogata

Vitrolfie K.K. Scientific support

sogata@vitrolife.com03-6459-4437

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026