An observational study in Recurrent Implantation Failure and Infertility (IVF Patients), sponsored by King's College London. Not yet recruiting at 1 site in United Kingdom. Open to female participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-30.
Sponsored by King's College London · Observational
The goal of this observational study is to learn whether differences in the immune cells of the womb lining (endometrium) help explain why some women do not become pregnant despite several IVF attempts using good-quality embryos, a condition known as recurrent implantation failure (RIF). The study compares women with RIF to women who have had a natural, healthy pregnancy. The main question it aims to answer is:
Do immune cells in the endometrium, including uterine natural killer cells, macrophages, B cells, and T cells, differ in number or function between women with RIF and fertile controls?
Researchers will compare endometrial tissue and blood samples from the RIF group to samples from the fertile control group to see whether specific immune cell patterns are linked to implantation failure, and whether these differences could point to future treatment targets.
Participants will:
Recurrent implantation failure (RIF) is a phenomenon specific to assisted reproductive technology, defined using the ESHRE threshold where the calculated cumulative chance of pregnancy exceeds 60 percent yet pregnancy does not occur without a known cause. True incidence is estimated at around 5 percent. While embryonic factors affecting implantation have been substantially addressed through developments such as preimplantation genetic testing for aneuploidy (PGT-A), there remains a lack of robust research into the uterine environment itself, hampered by inconsistent definitions and investigations without established evidence of benefit.
The immune system is known to mediate implantation by balancing pro-inflammatory and anti-inflammatory activity, both to permit implantation and to avoid rejection of the embryo. This study characterises the local, tissue-resident immune cell populations of the endometrium, examining not only the number of each immune cell type present but also their phenotype and function, using surface protein expression, transcriptomic profiling, and T cell receptor sequencing to assess activation state, functional subtype, and clonal expansion within each population.
Recruitment: RIF participants are identified at King's Fertility through internal database searches and clinical record review. Control participants who have had a spontaneous pregnancy are identified through review of 36 week gestation scan appointments at the Harris Birthright Centre, King's College Hospital, between 12 and 36 months prior. Eligible individuals are approached by a member of their direct care team by email and invited to a consent appointment, which can take place remotely.
Study procedure: The mid-luteal phase is identified using twice daily home urinary ovulation prediction tests from day 9 of the menstrual cycle. Participants attend a study visit 7 days after the luteinising hormone (LH) surge, where transvaginal ultrasound and venepuncture are used to confirm a corpus luteum and serum progesterone level consistent with the mid-luteal phase. An endometrial biopsy is then performed at the same visit under transabdominal ultrasound guidance. Where a participant consents to optional future use of samples, an additional blood sample of up to 18ml is collected on the same day, bringing total blood volume to up to 25ml where this option is taken. All procedures take place at King's Fertility, First Floor, The Fetal Medicine Research Institute, 16 to 20 Windsor Walk, Denmark Hill, London SE5 8BB.
Sample processing and analysis: Endometrial tissue and blood samples are transported to the King's College London Immunoregulation Laboratory, Guy's Campus, where endometrial biopsies are immediately cryopreserved and blood is processed to isolate cells from plasma before cryopreservation. Conventional flow cytometry and fluorescence activated cell sorting (FACS) are used for cell sorting and characterisation. CITE-seq (Cellular Indexing of Transcriptomes and Epitopes by sequencing) allows simultaneous analysis of transcriptomic and surface protein expression profiles. Single cell RNA sequencing on the 10x Genomics platform, including T cell receptor (TCR) sequencing, is performed to assess immune cell phenotype and clonal expansion. Raw sequencing data are processed using CellRanger and analysed in Seurat (R environment), producing transcriptomic profile, surface protein expression, and TCR repertoire data. Differential expression and clonality analyses compare immune cell phenotypes between the RIF and control groups, integrating gene expression, surface phenotype, and lineage.
Translational aim: This work is intended to build a high resolution reference atlas of the non-receptive endometrium, allowing stratification of individuals affected by RIF according to underlying immune aetiology, and to identify immune cells or pathways that could inform future immune modulating therapeutic approaches, whether through upregulation or downregulation of a specific immune pathway.
Women under 40 with recurrent implantation failure following IVF, identified through clinical records at King's Fertility (Denmark Hill and Harley Street), and women with a history of spontaneous pregnancy resulting in live birth, identified through 36-week gestation scan records at the Harris Birthright Centre, King's College Hospital. Both groups are drawn from patients already attending these services, approached by their direct care team if they have previously consented to research contact.
Recurrent Implantation Failure (RIF) Cohort:
Control Cohort:
Exclusion Criteria:
Recurrent Implantation Failure (RIF) Cohort:
Control Cohort (in addition to all RIF cohort exclusions above):
Women meeting the ESHRE definition of recurrent implantation failure (failure to achieve pregnancy despite an estimated cumulative chance of implantation exceeding 60%), with unexplained infertility, recruited through King's Fertility.
Women with a history of at least one spontaneous pregnancy resulting in live birth, at least 12 months postpartum, with no history of subfertility, recruited through the Harris Birthright Centre, King's College Hospital.
Th17/Treg ratio in the endometrium
Ratio of T helper 17 (Th17) cells to regulatory T (Treg) cells in endometrial tissue, measured by flow cytometry and single-cell RNA sequencing/CITE-seq, compared between participants with recurrent implantation failure (RIF) and fertile controls.
Time frame: Through study completion, up to 27 months
Reference atlas of endometrial immune cell populations
High-resolution profiling of endometrial-resident immune cell populations, including uterine natural killer cells, macrophages, B cells, and T cells, by single-cell RNA sequencing and CITE-seq, to identify transcriptomic and phenotypic patterns associated with implantation failure.
Time frame: Through study completion, up to 27 months
Candidate immune targets for future therapeutic research
Identification of immune cell populations, activation states, or clonal T-cell expansions that covary with the Th17/Treg axis and may represent candidate targets for future therapeutic research in recurrent implantation failure.
Time frame: Through study completion, up to 27 months
Plan to share: Yes — Pseudonymised individual participant data, including transcriptomic, proteomic, and T cell receptor sequencing data, may be deposited in a controlled-access repository and/or shared directly with other researchers upon reasonable request, subject to approval by the Chief Investigator, as data custodian, and King's College London's research governance office, and a formal data sharing agreement. Given the genomic nature of the data, full anonymisation is not possible; re-identification is only possible via a secure linkage key held by designated, authorised members of the research team. Processed or summary-level data not carrying re-identification risk may be made available more openly, for example as supplementary material accompanying publications.
Supporting information: Study protocol, Sap, Icf, Analytic code
No publications or documents are linked to this record.
This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
King's College London