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临床试验/NCT06650540
NCT06650540尚未招募不适用

Levofloxacin Plus Metronidazole Suppositories Versus Levofloxacin Co-administered with Metronidazole Tablets for the Treatment of Chronic Endometritis: a Randomized Controlled Trial

Peking University Third Hospital1 个研究点 分布在 1 个国家目标入组 800 人开始时间: 2024年10月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
800
试验地点
1
主要终点
live birth rate after the first embryo transfer

研究概览

简要总结

This is a single randomised controlled trial. The investigators plan to randomise 800 participants to the levofloxacin plus metronidazole suppositories versus levofloxacin co-administered with metronidazole tablets for the treatment of chronic endometritis in a 1:1 rate. Primary outcome will be the live birth rate after the embryo transfer.

详细描述

Chronic endometritis (CE) is a pathological condition characterized by inflammation and destruction of the endometrium. In this disease state, microorganisms coexist with the host's immune system in a balanced manner. However, for the majority of patients with CE, clinical symptoms are nonspecific and atypical, rendering diagnosis based on clinical signs or blood tests unreliable. Consequently, invasive procedures such as histopathological examination of the endometrium or hysteroscopy are often necessary to establish a definitive diagnosis. The infiltration of plasma cells in the endometrial stroma associated with CE, together with increased production of immunoglobulins and pro-inflammatory cytokines, can reduce endometrial receptivity. This reduction in receptivity can lead to an increased risk of female infertility, lower pregnancy rates, and reduced live birth rates, which are linked to unexplained infertility, repeated failure of embryo implantation, and recurrent miscarriages. While the etiology of CE remains elusive, it is widely believed to be related to infection by pathogenic microorganisms such as Streptococcus, Enterococcus faecalis, Escherichia coli, Staphylococcus , Klebsiella pneumoniae, Ureaplasma, and Mycoplasma, which can ascend from the vagina into the uterine cavity. Preliminary basic research by investigators also supports the notion that bacterial infections are a leading cause of endometritis. The mainstay of CE treatment currently involves oral antibiotics, with a common regimen being colabitux (500 mg once daily for 14 days) in combination with metronidazole (400 mg twice daily for 14 days). However, oral antibiotics can face issues such as drug resistance, suboptimal local concentrations of the drug, and a propensity to cause gastrointestinal side effects like nausea, vomiting, diarrhea, abdominal distension, and dermatological reactions like skin rashes and leukopenia, which can lead to treatment interruptions and reduced efficacy in managing chronic endometritis. Therefore, there is a need to explore methods to enhance the treatment success rate of CE. Metronidazole suppositories, composed primarily of metronidazole, are used vaginally to treat bacterial infections and other types of bacterial-induced vaginitis. Acting directly on the local area, these suppositories typically exhibit faster and more pronounced therapeutic effects without adversely affecting other tissues and organs. Given that the vagina is connected to the uterine cavity via the cervix, investigators hypothesized that local vaginal administration of the medication might be more effective. This approach not only achieves higher local concentrations of the drug in the uterine cavity, but also prevents ascending infection of vaginal bacteria.

In the prospective, randomized study conducted by investigators, the efficacy of levofloxacin plus metronidazole suppository versus levofloxacin co-administered with metronidazole tablets was compared in patients with chronic endometritis. By comparing the pregnancy outcomes of the two groups, the aim was to identify a superior treatment strategy, enhance treatment efficacy, and improve clinical outcomes.

Purpose The objective of this study is to investigate the efficacy of metronidazole therapy in enhancing treatment outcomes for chronic endometritis, with the aim of increasing clinical pregnancy and live birth rates in IVF procedures, reducing miscarriage rates, and thereby offering a safer and more effective treatment option for participants with chronic endometritis who are considering pregnancy.

Design This study is designed as a randomized controlled trial. Study Population

Inclusion Criteria:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 42 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Infertile patients aged 20-42 years
  • Hysteroscopy and endometrial biopsy were performed, and the
  • Pathological diagnosis was chronic endometritis
  • Serum FSH level on the second day of menstruation was ≤12U/L
  • Agree and sign the informed consent form

排除标准

  • Patients with the following diagnoses: submucosal myoma; Uterine malformation or previous surgery for correction of uterine deformity; Intrauterine adhesions; The previous history of pelvic tuberculosis or endometrial tuberculosis or the current pathology suggested endometrial tuberculosis; Endometrial hyperplasia or endometrial cancer
  • Patients with spouse, previous fetal or child chromosomal abnormalities who plan to undergo preimplantation genetic screening
  • Patients with a history of allergy to study drugs

研究组 & 干预措施

Levofloxacin Plus Metronidazole Suppositories group

Experimental

Clinical pregnancy outcomes of the first embryo transfer in patients with chronic endometritis treated with Levofloxacin Plus Metronidazole Suppositories.

干预措施: Levofloxacin Plus Metronidazole Suppositories (Drug)

Levofloxacin co-administered with Metronidazole tablets group

Active Comparator

Clinical pregnancy outcomes after the first embryo transfer in patients with chronic endometritis treated with Levofloxacin co-administered with Metronidazole tablets.

干预措施: Levofloxacin co-administered with Metronidazole tablets (Biological)

结局指标

主要结局

live birth rate after the first embryo transfer

时间窗: 22 weeks to 43 weeks gestation after the first embryo transfer cycle

Live birth is defined as the delivery of at least one baby after 22 weeks of gestation Oversight that exhibits any sign of life.

次要结局

  • Clinical pregnancy(around 7 weeks' gestation after the first embryo transfer cycle)
  • Ongoing pregnancy(12 weeks to 43weeks gestation after the first embryo transfer cycle)
  • Biochemical pregnancy(about 14 days after embryo transfer)
  • Miscarriage(6-22 weeks of gestation)
  • Cumulative live birth(6 monti after the first embryo transfer)
  • Pre-eclampsia(after 20 weeks of gestation)
  • Gestational hypertension(after 20 weeks of gestation)
  • Gestational diabetes mellitus(between 24 -28 weeks of gestation)
  • Premature rupture of membrane(PROM)rate(Time Frame: the day of delivery)
  • Preterm delivery(up to 37 weeks)
  • Placenta previa(the day of delivery)
  • Postpartum hemorrhage(the day of delivery)
  • Birth weight(the day of delivery)
  • Stillbirth(the day of delivery)
  • Mode of delivery(the day of delivery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lin MingMei

Professor

Peking University Third Hospital

研究点 (1)

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