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临床试验/NCT05670795
NCT05670795招募中不适用

Comparison of Recombinant Follicle Stimulating Hormone and the Combination of Recombinant Follicle Stimulating Hormone With Clomiphene Citrate in Stimulated Intrauterine Insemination Cycles: A Prospective Randomized Controlled Multicentric Study

Bezmialem Vakif University1 个研究点 分布在 1 个国家目标入组 254 人开始时间: 2023年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
254
试验地点
1
主要终点
Rate of clinical pregnancy

研究概览

简要总结

The aim of study is to evaluate the results of two different protocols for ovulation induction during IUI cycles. All patients undergo IUI cycles are randomly divided in to two groups. the first group is recombinant follicle stimulating hormone and the second group is the combination of recombinant follicle stimulating hormone with clomiphene citrate.

详细描述

Approximately %10-15 of couples of reproductive age, have infertility issues. %30-40 male factor, %40-50 female factor, and %20-25 both play a role in infertility etiology. Contributory factors of cases are %30-40 male factors, %40-50 female factors, and %20-25 mixed type. Ovulation induction and intrauterine insemination (IUI) are the main treatments for infertility. IUI is accepted as the most used treatment procedure according to other assisted reproductive techniques because it has lower costs, can be easily applied, and is less invasive. Clomiphene citrate is the most commonly used for ovulation induction, which is cheaper and has a lower incidence of multiple pregnancies. Controlled ovarian hyperstimulation with recombinant follicle stimulating hormone and IUI has a higher incidence of pregnancy rates in an ovulation, unexplained and mild male factor infertility cases.

Data including age, BMI, smoking, the duration of infertility, the type of infertility, total motile sperm count (TMSS) of inseminated material and sperm morphology, antral follicle count, number of developed follicles and endometrial thickness on HCG day will be recorded. On the 2nd or 3rd day of the cycle, the patient will be randomized into two groups. Group 1 (rFSH: n=127, 75 IU FSH/day), and Group 2 (clomiphene citrate 100 mg/day for 5 days following by 75 IU FSH/day; n=127). Human chorionic gonadotropin (hCG) will be used for trigger when the dominant follicle's diameter reaches 17-18mm for ovulation. Thirty-six hours after the hCG injection, single IUI will be performed by using the fresh sperm obtained by the density gradient method with a soft catheter in the dorsolithotomy position under ultrasound guidance. The patient will be kept supine position after the procedure for 15 minutes. After IUI, sexual intercourse will be recommended for three days. Intravaginal progesterone (LUTINUS® 100 mg vaginal tablet, Ferring GmbH Wittland/Kiel/Germany) to both groups will be used once a day after insemination for luteal phase support. Clinical pregnancy rates will be recorded by performing a blood test for on the 15th day after the procedure.

The aim of study is to evaluate the results of two different protocols for ovulation induction during IUI cycles. All patients undergo IUI cycles are randomly divided in to two groups. the first group is recombinant follicle stimulating hormone and the second group is the combination of recombinant follicle stimulating hormone with clomiphene citrate

研究设计

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

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 18-40 years old female
  • Unexplained infertility
  • Regular menstrual cycle
  • Bilateral tubal patency in HSG and normal uterine cavity
  • Total motile sperm count greater than 10 million/ml

排除标准

  • History of ovarian surgery
  • Uncorrected uterine pathology
  • Other endocrine diseases (thyroid, prolactin, hypogonadotropic hypogonadism)
  • Presence of a cyst greater than 10 mm on USG in 2-3 days of the period
  • Stage 3-4 endometriosis
  • TMSS < 5 million/ml on the insemination day
  • Conditions where rFSH and clomiphene citrate are contraindicated

研究组 & 干预措施

recombinant follicle stimulating hormone

Experimental

Gonal-f® (75 I.U., Merck Serono, Darmstadt, Germany)

干预措施: Recombinant Follicle Stimulating Hormone (Drug)

recombinant follicle stimulating hormone and clomiphene citrate

Active Comparator

Gonal-f® (75 I.U., Merck Serono, Darmstadt, Germany) Klomen® (50 mg, Koçak Farma, Tekirdag, Turkey)

干预措施: Recombinant Follicle Stimulating Hormone and Clomiphene Citrate (Drug)

结局指标

主要结局

Rate of clinical pregnancy

时间窗: day 15

after iui betahcg levels blood sampling

次要结局

  • Rate of ongoing pregnancy(Months 3)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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