跳至主要内容
临床试验/NCT02700256
NCT02700256已完成不适用

Electronic Patient-Reported Outcomes in Patients Recovering From Ambulatory Cancer Surgery: Measuring Early Postoperative Symptoms

Memorial Sloan Kettering Cancer Center5 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2015年12月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
135
试验地点
5
主要终点
number of patients who respond to the survery

研究概览

简要总结

The purpose of this pilot study is to find out if patients are willing to self-report symptoms in the first 5 days following discharge, or when they leave the hospital after "ambulatory surgery" ("ambulatory surgery" is when the patient has surgery and then goes home within 24 hours).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • The patients must be undergoing surgery for an indication tracked within the Gynecologic AXR program or have an expected postoperative discharge within 24 hours of surgery. These surgical procedures typically include: minimally invasive hysterectomy or radical hysterectomy, salpingo-oophorectomies [mentioned above], and minimally invasive staging procedures.
  • The patient must have a phone number or an email address.
  • The patient must be willing to self-report postoperative symptoms over an automated phone system or via an online platform.
  • The patient must speak and read fluent English.

排除标准

  • Non-English speaking patients
  • Patients unwilling to provide contact information (email or phone number)

结局指标

主要结局

number of patients who respond to the survery

时间窗: up to 5 days after surgery

A patient will be deemed a "responder" if they complete at least 5 of the 8 symptom items on at least 3 days postoperatively. The symptom assessment method will be deemed successful if 32 of the 50 patients respond.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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