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临床试验/NCT06268587
NCT06268587已完成不适用

A Before and After Study Studying the Impact of an Analgesia Protocol After Discharge From Outpatient Surgery

Centre Hospitalier Universitaire de Liege1 个研究点 分布在 1 个国家目标入组 1,423 人开始时间: 2019年9月1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
1,423
试验地点
1
主要终点
Measure the impact of the protocol on the proportion of patients with a pain greater than 3/10 on a Visual Analogue Scale at day one and who did not take the analgesics.

研究概览

简要总结

The goal of this before and after study is to measure the effectiveness of a home analgesia protocol after outpatient surgery in a tertiary hospital. The main question it aims to answer is:

  • Measure the impact of the protocol on the proportion of patients with a VAS greater than 3/10 on day one and who did not take the analgesics.

The participants are divided into two groups. The control group leaves the hospital with instructions and prescriptions. The experimental group leaves the hospital with instructions, analgesics for a maximum of two days with detailed dosages and an explanatory booklet on postoperative pain.

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • outpatient surgery
  • no age limit
  • accepted post-operative monitoring by text messages (SMS)

排除标准

  • refusal of post-operative follow-up by text messages (SMS)

结局指标

主要结局

Measure the impact of the protocol on the proportion of patients with a pain greater than 3/10 on a Visual Analogue Scale at day one and who did not take the analgesics.

时间窗: day 1

Visual Analogue Scale = 0/10 : no pain Visual Analogue Scale = 10/10: maximal pain The patients receive a text message (SMS) on day 1 asking for their pain level between 1 and 10. They send the response via SMS. If the response is greater than 3/10, an SMS asks patients if they have taken their painkillers. If they took them, they say "taken". Otherwise, they are invited to take them and are contacted again 45 minutes later for a new evaluation. In the event of no response to the SMS or pain \> 3/10 despite taking the prescribed painkillers, they are contacted by telephone.

次要结局

  • Measure the impact of the protocol on the occurrence of nausea and vomiting on day one(day 1)
  • Measure the adequacy of post-op analgesics by measuring the proportion of patients with a Visual Analogue Scale < or = 3/10 on day one for each group(day 1)
  • Measure the impact of the protocol on general satisfaction of stay in outpatient surgery on day 7 with a Visual Analogue Scale Satisfaction(day 7)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Samalea Suarez Nicolas, MD

MD

Centre Hospitalier Universitaire de Liege

研究点 (1)

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