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临床试验/NCT01848847
NCT01848847已完成不适用

The Impact of Bladder Distention on Execution of Diagnostic Hysteroscopy Procedure; a Randomised Controlled Trial.

Namik Kemal University1 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2013年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
102
试验地点
1
主要终点
Ease of Cervical Entry

研究概览

简要总结

The purpose of the study is to investigate the advantages and disadvantages of bladder filling during hysteroscopy procedure.

详细描述

Women who should have diagnostic hysteroscopy procedure will be randomly allocated into two groups. In the first group hysteroscopy will be performed with a filled bladder and in the second group procedure will be performed with an empty bladder. The women will be assigned into groups randomly. The duration of the procedure, feasibility of the procedure and tolerability of procedure will be recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Investigator)

入排标准

年龄范围
17 Years 至 55 Years(Child, Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Women who are at reproductive age
  • •Women who are not pregnant at the time of presentation
  • •Women who are not nulliparous

排除标准

  • •Women who have previous cervical surgery or cervical incompetence.
  • •Women who have genitourinary infection
  • •Women who have profuse uterine bleeding or recent uterine perforation
  • •Women who have neurological disorders affecting evaluation of pain.

研究组 & 干预措施

Empty Bladder

Experimental

Hysteroscopy conducted under empty bladder.

干预措施: Hysteroscopy (Procedure)

Full Bladder

Experimental

Hysteroscopy conducted under full bladder.

干预措施: Hysteroscopy (Procedure)

结局指标

主要结局

Ease of Cervical Entry

时间窗: 2 months

Ease of cervical entry which will be assessed by Likert scale.The outcome measures in this study were the ease of cervical entry (judged by the individual surgeons using a 5-point Likert scale: very difficult= 1, difficult= 2, fair = 3, easy= 4, and very easy = 5.

Pain Scoring(VAS)

时间窗: 2 months

Pain scoring was made by 10 cm visual analog scale. pain score (recorded by the patient on a 10 -point visual analog scale (VAS) which means pain increases with increasing number

次要结局

  • Patient Acceptability and Pain Scoring(two months)
  • Procedure Duration(two months)

研究者

发起方
Namik Kemal University
申办方类型
Other
责任方
Principal Investigator
主要研究者

CEM CELIK

Assistant Professor

Namik Kemal University

研究点 (1)

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