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临床试验/NCT06979583
NCT06979583Enrolling By Invitation不适用

Impact of Ureteral Stent Size on the Management of Post Ureteroscopy Pain: a Randomized Single Blind Trial

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2027年3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
Enrolling By Invitation
发起方
Mayo Clinic
入组人数
100
试验地点
1
主要终点
Pain score post ureteroscopy procedure until stent removal determined by the primary operating team. Stent will be on a string

研究概览

简要总结

The purpose of this study is to determine if post-operative stent size impacts stent-related pain and discomfort.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients undergoing a retrograde intra-renal surgery (RIRS) (only patients undergoing the procedure for stone treatment will be included) who will require post-operative indwelling ureteral stent placement on a string at the conclusion of the procedure.

排除标准

  • •Patients with intra-operative ureteral injury who will require ureteral stent for extended time (more than 10 days, in that case a stent without a string will be used).
  • •Patient undergoing ureteroscopy for any indication other than stone extraction.
  • •Patients who are currently pregnant as determined by clinical presurgical screening.

研究组 & 干预措施

Group B: 7 Fr Ureteral stents

Experimental

干预措施: 7 Fr Ureteral stents (Device)

Group A: 4.8 Fr Ureteral stents

Experimental

干预措施: 4.8 Fr Ureteral stents (Device)

结局指标

主要结局

Pain score post ureteroscopy procedure until stent removal determined by the primary operating team. Stent will be on a string

时间窗: Starting post-operatively, daily, until stent is removed (estimated 7-14 days)

Post-operatively, patient will be contacted by study coordinators every day until stent is removed (usually 7-14 days after the surgery) to scale their stent pain on a scale from 1-5 as following: No pain: 1; Mild pain with no need for additional medication: 2; Mild pain with need for additional medication (anticholinergics): 3; Moderate stent pain (requiring narcotics): 4; Severe stent pain (requiring ER visit): 5.

次要结局

  • Volume of post-operative correspondence between patients and medical system.(14 days)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Sponsor
主要研究者

Meghan A. Cooper

Principal Investigator

Mayo Clinic

研究点 (1)

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