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临床试验/NCT03604549
NCT03604549已完成4 期

Therapeutic Effect of Sonographic Hysterosalpingography: Oil vs Water Based Media

Milton S. Hershey Medical Center1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2019年1月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
58
试验地点
1
主要终点
Ongoing Pregnancy Rate

研究概览

简要总结

Performing fluoroscopic HSG with oil based contrast medium has been shown to increase pregnancy rates in a subfertile population. This is a pilot study to test the efficacy of as well as the tolerability and safety of using lipid based oil medium for sonographic based hysterosalpingography (Sono HSG) compared to water based contrast (i.e. normal saline) for women seeking fertility. The double blind study will randomize 56 women at the time of Sono HSG in a 1:1 ratio to receive through the SHG catheter either up to 10 cc of Lipiodol UF® or normal saline. The investigators will collect subjective pain experience and follow the subjects for 6 months after the test for pregnancy and collect all adverse events during and after the procedure.

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
Triple (Participant, Care Provider, Investigator)

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

  • Eligible for Sono HSG for fertility testing
  • In good general health
  • Willing and capable of complying with the study procedures
  • At least one patent tube and no endometrial pathology on Sono HSG
  • Ready to undergo infertility treatment immediately after the test
  • Not planning on IVF therapy in the next 6 mos

排除标准

  • Known tubal or endometrial (polyp, submucous fibroid, etc.) pathology
  • At high risk for tubal disease due to history of Pelvic Inflammatory Disease
  • Known hypersensitivity to Lipiodol UF®or known allergy to iodine containing contrast media or shellfish
  • Endometrial pathology on Sono HSG requiring further evaluation (as per the performing physician)
  • Bilateral tubal occlusion on Sono HSG
  • Unable to tolerate potential pain associated with the study.
  • Requiring IVF due to severe male factor, known pelvic adhesions, etc.
  • Couples with decreased male factor fertility rate (i.e., low sperm count or motility, i.e. less than 5 million/mL concentration on semen analysis

研究组 & 干预措施

Saline

Placebo Comparator

Women in this arm will receive a flush with saline after normal saline Sono HSG.

干预措施: Saline (Drug)

Lipiodol UF

Experimental

Women in this arm will receive a flush with Lipiodol UF after normal saline Sono HSG.

干预措施: Lipiodol UF (Drug)

结局指标

主要结局

Ongoing Pregnancy Rate

时间窗: within 6 months of Sono HSG procedure

8 week viable intrauterine pregnancy

次要结局

  • Procedural Related Pain Assessed by Visual Analog Scale(After sono hystersalpingography study infusion/procedure completed)

研究者

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

Richard S. Legro, M.D.

Interim Chair and Vice Chair of Research, Department of Obstetrics and Gynecology, Professor of Obstetrics and Gynecology and Public Health Sciences

Milton S. Hershey Medical Center

研究点 (1)

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