Overview

Improvement of Live Babies Rates After ICSI, Using cpFT

Status:
Not yet recruiting
Trial end date:
2024-08-26
Target enrollment:
0
Participant gender:
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 3
Accepts Healthy Volunteers?
No
Details
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