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Preimplantation Genetic Screening in IVF Treatment

Preimplantation Genetic Testing for Aneuploidy (PGT-A) in in Vitro Fertilisation (IVF) Treatment: Pilot Phase of a Randomised Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05009745
Acronym
PGSINIVF
Enrollment
100
Registered
2021-08-17
Start date
2021-06-10
Completion date
2023-02-28
Last updated
2021-08-17

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

Conditions

Infertility

Keywords

Preimplantation Genetic Testing, IVF, RCT, Pilot Study

Brief summary

This is the pilot phase of a randomised controlled trial. The purpose of the pilot study is to assess the ability to recruit, randomise, adherence to the study protocol and plan for a full study. The purpose of the full study will be to determine if a policy of embryo selection and transfer based on morphological evaluation and preimplantation genetic testing for aneuploidy (PGT-A) is a more clinically effective, safer, cost-effective and acceptable way to provide in vitro fertilisation (IVF) treatment in women of advanced reproductive age compared to the routine practice of embryo selection and transfer based on morphological evaluation alone.

Detailed description

The target population for the trial are women aged 35 - 42 years undergoing IVF±ICSI treatment. Intervention The experimental strategy will be to perform PGT-A (also referred as preimplantation genetic screening - PGS) involving trophectoderm biopsy on embryos reaching the blastocyst stage on day 5/6/7 following egg collection. All embryos will be frozen after the biopsy procedure. Comprehensive chromosome screening (CCS) of all chromosomes will be performed using next generation sequencing (NGS). Embryos will be categorised as euploid, mosaic euploid and aneuploid embryos and embryos will be ranked based on the degree of euploidy. Only euploid embryos or mosaic euploid embryos deemed suitable to be replaced will be transferred in subsequent frozen-thawed embryo transfer cycles. Comparison Women in the control arm will have the fresh embryo transfer procedure on day 5 following egg collection or a frozen-thawed embryo transfer as first line if clinically indicated in keeping with current routine practice. Embryo selection for transfer will be based on morphological criteria alone.

Interventions

PROCEDUREPGT-A Strategy

PGT-A strategy involves trophectoderm biopsy, comprehensive chromosome screening (CCS) using Next Generation Screening (NGS), freezing of embryos and replacement in a frozen-thawed embryo transfer cycle.

Sponsors

Guy's and St Thomas' NHS Foundation Trust
CollaboratorOTHER
King's College London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Masking description

The participants, care providers, investigators and outcome assessors will not be masked.

Intervention model description

Pilot phase of a prospective, allocation concealed two arm parallel RCT

Eligibility

Sex/Gender
ALL
Age
35 Years to 42 Years
Healthy volunteers
Yes

Inclusion criteria

* Inclusion criteria for the study would be women aged 35 - 42 years undergoing IVF ± ICSI for treatment of infertility * Patients with 3 or more good quality embryos (assessed according to the embryo scoring system of the Association of Clinical Embryologists, UK) on day 3 following egg collection * Ability to provide informed written consent

Exclusion criteria

* Women undergoing preimplantation genetic testing for inherited genetic disorders * Gamete donation cycles * Untreated hydrosalpinges * Untreated uterine pathology (eg: endometrial polyps, submucous fibroids, intramural fibroids \> 5 centimetres in maximum diameter, intrauterine adhesions, uterine septa)

Design outcomes

Primary

MeasureTime frameDescription
Recruitment rate18 monthsPilot phase RCT with an aim to progress to a multi-centre RCT

Secondary

MeasureTime frameDescription
Clinical pregnancy rate21 monthsClinical pregnancy is defined as presence of an intrauterine gestational sac with a foetal pole and heart beat identified by ultrasound scan.

Countries

United Kingdom

Contacts

Primary ContactSponsor Representative
R&D@gstt.nhs.uk+44 2071889811

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026