跳至主要内容
临床试验/NCT05571072
NCT05571072已完成不适用

Opioid Use After Urogynecologic Procedures: Using a Predictive Calculator

David Sheyn1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2023年1月2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
110
试验地点
1
主要终点
Change in pain scores measured by team-created pain questionnaires

研究概览

简要总结

The purpose of this study is to determine if the investigators can precisely predict how much pain medication the subjects will need after surgery using a special calculator that was developed for this purpose.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Age 18-89
  • •Able to provide informed consent
  • •Patients undergoing any of below urogynecologic procedures
  • •Included urogynecologic procedures:
  • •Sacrocolpopexy - robotic or laparoscopic
  • •With or without hysterectomy
  • •With or without salpingo-oophorectomy
  • •With or without anterior colporrhaphy
  • •With or without posterior colporrhaphy/perineorrhaphy
  • •With or without midurethral sling
  • •Sacrospinous ligament fixation
  • •With or without hysterectomy
  • •With or without salpingo-oophorectomy
  • •With or without anterior colporrhaphy
  • •With or without posterior colporrhaphy/perineorrhaphy
  • •With or without midurethral sling
  • •Uterosacral ligament suspension - robotic, laparoscopic, or vaginal
  • •With or without hysterectomy
  • •With or without salpingo-oophorectomy
  • •With or without anterior colporrhaphy
  • •With or without posterior colporrhaphy/perineorrhaphy
  • •With or without midurethral sling
  • •Colpocleisis
  • •Lefort colpocleisis
  • •Complete colpectomy with colpocleisis
  • •Isolated anterior and/or posterior colporrhaphy

排除标准

  • •Non-English speakers
  • •pre-operative diagnosis of cancer
  • •scheduled for any concurrent non-urogynecologic procedure (ex: abdominoplasty)
  • •<18 years or >89 years of age
  • •unable to provide informed consent

研究组 & 干预措施

Standard Opioid Prescription

Active Comparator

Patients will be given a prescription for opioid pain medication to use for acute postoperative pain as would be typical for the attending surgeon performing the surgery.

干预措施: Standard opioid prescription (Other)

Opioid Calculator Prescription

Experimental

Patients will be a given a prescription for opioid pain medication based on the opioid calculator.

干预措施: Opioid calculator (Other)

结局指标

主要结局

Change in pain scores measured by team-created pain questionnaires

时间窗: baseline, 1 week post-op, 2 weeks post-op

Pain questionnaire is a 2 question survey that ask patients to rate pain on scale of 0 (no pain) to 10 (worst pain) immediately post-op and current. Baseline will be calculated by asking patient's expected post-op pain score.

次要结局

  • Change in satisfaction scores measured by team-created questionnaire(1 week post-op, 2 weeks post-op)
  • Change in number of opioid tablets remaining measured by team-created questionnaire(1 week post-op, 2 weeks post-op)

研究者

发起方
David Sheyn
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

David Sheyn

Associate Professor of Urology

University Hospitals Cleveland Medical Center

研究点 (1)

Loading locations...

相似试验