Chronic Endometritis and IVF

in Vitro Fertilization Clinical Trial

— CEIVF  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02646930
• Other study ID #: Pro00067725
• Status: Completed
• Phase: N/A
• Start date: March 3, 2016
• Est. completion date: May 16, 2019

Study information

• Verified date: October 2020
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 57
• Est. completion date: May 16, 2019
• Est. primary completion date: May 16, 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 21 Years to 35 Years

Eligibility

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 TNFa 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.

Related Conditions & MeSH terms

• Chronic Endometritis
• Endometritis
• in Vitro Fertilization

Intervention

Procedure:
• Endometrial biopsy
Endometrial biopsy in women undergoing first IVF cycle

Locations

Country	Name	City	State
United States	University of Illinois	Chicago	Illinois
United States	Duke Fertility Clinic	Durham	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Duke University	University of Illinois at Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Ongoing pregnancy rate		12 weeks gestation
Secondary	Implantation rate		12 weeks
Secondary	Pregnancy loss rate		12 weeks