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NCT Number: NCT02646930

Chronic Endometritis and IVF

Background: Embryo quality is known to be a very important determinant to predict the implantation and pregnancy rate in IVF patients, however, the role of uterine integrity or endometrial receptivity cannot be overlooked.

Chronic endometritis (CE) is an inflammation of the endometrium diagnosed by the presence of plasma cells in the endometrial stroma. There is not only no census on the definition of CE, the current literature on the impact of CE on reproductive outcome is controversial and consists only of retrospective studies with small sample sizes. Although there is a presumption that CE is related to poor IVF outcome, this belief has not been proven.

Design: Prospective cohort study

Setting: Infertility clinics of 2 academic medical centers

Patients: Patients between the ages of ≥ 21 and ≤ 35 years old undergoing their first IVF cycle will be invited to participate.

Main Outcome Measures: The primary outcome will be ongoing pregnancy after 12 weeks estimated gestational age (EGA) with previously documented fetal cardiac motion. Secondary outcomes will include pregnancy loss rate as defined by chemical pregnancy, blighted ovum or loss of fetal cardiac motion before 12 weeks EGA.

Materials and Methods: The cycle prior to IVF, patients will undergo an in-office endometrial biopsy on cycle days 19-24. Samples will be stained for CD138 and the number of plasma cells will be quantified. The number of plasma cells in a sample that yields the best sensitivity and specificity for pregnancy will be determined by a Receiver-Operator-Curve. This number will then be used as a dichotomous variable to assign categories of "positive for CE" and "negative for CE." Pregnancy and miscarriage rates will then be determined in the positive and negative CE sample with Chi Square Analysis. A secondary sub analysis will be performed to determine pregnancy and miscarriage rates in patients who declined to participate in the study.

Expected Results: The investigators hypothesize that higher rates of CE will be found in women failing to conceive with IVF and with subsequent first-trimester miscarriage.

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Key information

Age range

21 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Illinois, Chicago, Illinois, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age of ≥ 21 and ≤ 35 years old
  • undergoing first IVF cycle
  • a diagnosis of ovulatory dysfunction, pelvic factor, male factor, cervical factor or unexplained infertility

Exclusion criteria

  • BMI > 40 kg/m2, anti-mullerian hormone (AMH) < 1.0 ng/mL or antral follicle count <10
  • previous endometrial ablation
  • previous uterine artery embolization
  • presence of type 0, 1, 2, 3 fibroid tumor
  • presence of type 4 fibroid tumor with a mean diameter of > 4 cm
  • presence of uterine anomaly other than arcuate configuration
  • presence of an endometrial polyp or endometrial synechiae
  • presence of a hydrosalpinx on hysterosalpingography or ultrasound
  • positive gonorrhea and chlamydia DNA testing
  • Patients on chronic glucocorticoids (except nasal preparations), or using glucocorticoids for assisted hatching will be excluded.
  • Patients on monoclonal antibody preparations directed to TNFα will be excluded.
  • Post-enrollment exclusion will include patients receiving any antibiotics, except prophylaxis for transvaginal oocyte retrieval (TVOR) or glucocorticoids, except nasal preparations, from the time of endometrial biopsy until initial transvaginal ultrasound (TVUS) for pregnancy.

Treatment and study plan

endometrial biopsy

Procedure

Endometrial biopsy in women undergoing first IVF cycle

Primary outcomes

  1. Ongoing pregnancy rate

    Time frame: 12 weeks gestation

Secondary outcomes

  1. Implantation rate

    Time frame: 12 weeks

  2. Pregnancy loss rate

    Time frame: 12 weeks

Sponsors and collaborators

Lead sponsor

Duke University

Other

Collaborators

  • University of Illinois at Chicago

Registry information

Official study title

The Impact of Chronic Endometritis on IVF Pregnancy and Pregnancy Loss Rates

Acronym: CEIVF

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Jan 6, 2016
Registry last updated
Oct 14, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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