Clinical Trial on the Methodology of Hysterosalpingography: a Comparative Study (MethodHSG)
研究概览
地位
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Istanbul、土耳其(türkiye)、34214
- Istanbul Medipol University, Medipol Mega University Hospital
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参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Female patients with infertility
Exclusion Criteria:
- Male patients
- Patients who are diagnosed with menopause
- Patients who do not want to proceed with HSG for diagnosis purposes
学习计划
研究是如何设计的?
设计细节
- 主要用途:卫生服务研究
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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有源比较器:Group 1: Metal Cannula
Applied to 158 infertile women.
While the patient was made to cough forcefully, a tenaculum was gently inserted into the cervix.
A Rubin cannula, de-aired and filled with radiopaque, was placed in the cervical canal.
The speculum was removed.
Traction was applied to the tenaculum to bring the uterus into a straight position, and while radiopaque material was injected under fluoroscopy, the cavity, tubal corneum, isthmus, ampulla, and degree of spillage into the abdomen were visualized.
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Different techniques of hysterosalpingography (HSG) were applied for 3 groups in parallel.
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有源比较器:Group 2: Active Method Balloon Catheter
Applied to 50 infertile women.
In this case, a balloon catheter was placed from the cervix into the uterine cavity.
A 2cc balloon was inflated.
The uterus was brought to a straight position by applying traction to the balloon catheter, and the cavity, tubal corneum, isthmus, ampulla, and degree of spillage into the abdomen were visualized while radiopaque material was injected under fluoroscopy guidance.
The uterine isthmus was visualized while the balloon was being deflated and withdrawn.
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Different techniques of hysterosalpingography (HSG) were applied for 3 groups in parallel.
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有源比较器:Group 3: Passive Method Balloon Catheter
Applied to 43 infertile women.
In this case, a balloon catheter was placed from the cervix into the uterine cavity.
A 2cc balloon was inflated.
While the balloon catheter was in the cavity, the tubal corneum, isthmus, ampulla, and degree of spillage into the abdomen were visualized by first injecting radiopaque material under fluoroscopy guidance.
Then, the cavity was visualized while the balloon catheter was being deflated and withdrawn, and the uterine isthmus was visualized.
This procedure was called the passive method balloon catheter method.
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Different techniques of hysterosalpingography (HSG) were applied for 3 groups in parallel.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Patient Satisfaction
大体时间:Day 1
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Patients' visual analogue scores (VAS) immediately after the procedure and 30 minutes post-procedure are recorded, respectively. The pain is assessed by the principal investigator. The visual analog scale for pain is a straight line with one end meaning no pain and the other end meaning the worst pain imaginable. The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10 cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be'). |
Day 1
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Clinician's Interpretation
大体时间:Day 1
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The interpretation is classified as "clearly evaluated", "partially evaluated" and as "could not be evaluated" by the clinician.
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Day 1
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合作者和调查者
调查人员
- 首席研究员:Gulseren Polat, M.D.、Medipol University
出版物和有用的链接
一般刊物
- Pellerito JS, McCarthy SM, Doyle MB, Glickman MG, DeCherney AH. Diagnosis of uterine anomalies: relative accuracy of MR imaging, endovaginal sonography, and hysterosalpingography. Radiology. 1992 Jun;183(3):795-800. doi: 10.1148/radiology.183.3.1584936.
- Preutthipan S, Linasmita V. A prospective comparative study between hysterosalpingography and hysteroscopy in the detection of intrauterine pathology in patients with infertility. J Obstet Gynaecol Res. 2003 Feb;29(1):33-7. doi: 10.1046/j.1341-8076.2003.00068.x.
- Chalazonitis A, Tzovara I, Laspas F, Porfyridis P, Ptohis N, Tsimitselis G. Hysterosalpingography: technique and applications. Curr Probl Diagn Radiol. 2009 Sep-Oct;38(5):199-205. doi: 10.1067/j.cpradiol.2008.02.003.
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- E-10840098-772.02-275
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Data is available upon reasonable request from the principal investigator, Dr. Gulseren Polat.
The results are planned to be published in a medical journal.
IPD 共享时间框架
IPD 共享访问标准
IPD 共享支持信息类型
- 研究方案
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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