Overview
Improvement of Live Babies Rates After ICSI, Using cpFT
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2024-08-26
2024-08-26
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
Demonstrate the improvement of the live births rate after ICSI by supplementing the pre-ICSI incubation medium of oocytes and that of preimplantation embryos with cpFT at the 1st embryo transfer for women under 37 years old.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Criteria
Inclusion Criteria:- Couples eligible for a first attempt at Assisted Reproduction (AMP).
- Couples asking for Assisted Reproductive Technology, and requiring an ICS procedure.
- Women aged 18 to 36 inclusive.
- Men aged 18 to 58 inclusive
- Use of CSCM-C culture medium from Biocare / Irvine, exclusively.
- People affiliated to a Social Security scheme
Exclusion Criteria:
- Lack of consent
- Early menopause.
- Couples under IVF or Intra Uterine Insemination treatment.
- Patients resumed after a first attempt by the couple.
- People unable to follow protocol visits in France.
- Couple with a contraindication to treatment with ART.
- Women with a contraindication to treatment with ART or an associated pathology such
as: hypertension, risk of eclampsia, viral risk, family genetic problems, diabetes,
uterine partitions, synechiae adhesions, adenomyosis or any other contraindication
judged as such by the investigator.
- AMP with donation of gametes or embryos.
- Frozen sperm.
- Participant under guardianship or guardianship