Fertility Outcomes After Antibiotic Treatment In Women With Chronic Endometritis

Recruiting now

Conditions studied: Endometritis, Infertility, Hysteroscopy, Pregnancy Disease

In brief

Chronic endometritis (CE) is a long-lasting inflammation of the lining of the uterus. Many women with CE do not have symptoms, but the condition may affect fertility, embryo implantation, and pregnancy outcomes. CE is usually diagnosed during hysteroscopy, a procedure that allows doctors to look inside the uterus and collect a small tissue sample for laboratory testing. The goal of this prospective cohort study is to learn how common CE is in women with infertility and to determine whether antibiotic treatment improves reproductive outcomes. The study will also examine whether hysteroscopic findings match laboratory-confirmed CE and whether certain findings can help doctors diagnose CE more accurately. In addition, researchers will study the types of bacteria found in the uterine lining and their possible relationship to fertility and pregnancy outcomes. The main questions the study aims to answer are: * How common is chronic endometritis in women undergoing infertility evaluation? * Does antibiotic treatment improve fertility and pregnancy outcomes in women with CE? * Can hysteroscopic findings reliably predict CE confirmed by laboratory testing? * Are specific bacteria associated with poorer reproductive outcomes? Researchers will enroll approximately 100 women aged 18 to 40 years with diagnosed infertility who are scheduled for hysteroscopy and endometrial biopsy as part of infertility evaluation. Participants with severe systemic disease, pregnancy, inability to undergo hysteroscopy or antibiotic treatment, or allergy to study antibiotics without a suitable alternative will not be included. Participants will: * Undergo diagnostic hysteroscopy and endometrial biopsy * Have tissue samples examined using histopathology and immunohistochemistry to identify CE * Receive standardized antibiotic treatment if CE is confirmed * Be followed for up to 12 months after treatment to monitor fertility outcomes * Continue follow-up during pregnancy, if pregnancy occurs, to assess pregnancy and delivery outcomes Researchers will evaluate spontaneous pregnancies, embryo transfer success, implantation rates, miscarriage rates, time to pregnancy, and live birth outcomes. Pregnancy complications such as preeclampsia, placental disorders, premature rupture of membranes, and preterm birth will also be recorded. The study is expected to run from January 2026 through December 2029. Data collected during the study may help improve the diagnosis and treatment of chronic endometritis in women with infertility and may support better reproductive outcomes in clinical practice.

Key facts

Study ID: NCT07603492
Run by: Faculty Hospital Kralovske Vinohrady
People needed: 100
Starts: 2026-01-01
Expected to finish: 2030-01-01
Last updated by the study team: 2026-05-27

Who can join

Age: 18 and older, up to 40. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

Female participants aged 18-40 years.
Diagnosis of infertility (primary or secondary infertility).
Indication for diagnostic hysteroscopy with endometrial biopsy as part of infertility evaluation.
Suspected or confirmed chronic endometritis.
Ability and willingness to provide written informed consent prior to any study-related procedures.
Willingness to undergo protocol-defined antibiotic treatment.
Willingness to comply with study procedures and follow-up assessments.
Agreement to reproductive outcome monitoring following treatment, including spontaneous conception and pregnancies achieved through assisted reproductive technologies (ART).

You may not qualify if…

Age >40 years.
Current pregnancy.
Known hypersensitivity or contraindication to tetracycline antibiotics or other study-related antibiotic therapy without a suitable alternative treatment option.
Severe systemic disease or medical condition that, in the opinion of the investigator, could interfere with study participation, safety, or interpretation of study results.
Active malignant disease requiring systemic treatment.
HIV infection or other severe immunodeficiency disorder.
Acute pelvic inflammatory disease or clinically significant active genital tract infection requiring immediate treatment.
Previous participation in this study.
Inability to undergo planned hysteroscopy or endometrial biopsy.
Inability or unwillingness to comply with study procedures or follow-up requirements.
Failure or refusal to provide written informed consent.

Where it is running

Faculty Hospital Královské Vinohrady — Prague, Czechia (enrolling)
PRONATAL Sanatorium — Prague, Czechia (enrolling)

Full record on ClinicalTrials.gov

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