跳至主要内容
临床试验/NCT06664242
NCT06664242已完成不适用

Effects of TENS Application in Patients Admitted to the ICU After Cardiac Surgery: a Randomized Double-blind Clinical Trial

Universidade Federal de Pernambuco2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年5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
10
试验地点
2
主要终点
respiratory muscle strength

研究概览

简要总结

Cardiac Surgery (CH) aims to increase survival and improve quality of life in eligible cardiac patients. However, as with any invasive intervention, pain is one of the main complaints of patients in the post-surgical period. This research is justified by the evaluation of the potential impact of the use of TENS as an alternative for analgesia in reducing the length of hospital stay and directly in the effective cost of patients undergoing cardiac surgeries, in reducing morbidity and mortality, as well as in the quality of life and early return to their daily activities, in addition to reducing the use of drugs and potentially their side effects. The objective of this study is to evaluate the effect of TENS for analgesia in hospitalized patients undergoing cardiac surgery, investigating its efficacy, safety and impact on postoperative recovery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Patients of both sexes
  • over 18 years of age,
  • undergoing elective cardiac surgery,
  • who have a sternotomy access route,
  • with or without the use of pleural or mediastinal drains,
  • after the first postoperative day will be selected.

排除标准

  • with unstable angina,
  • patients with arrhythmias,
  • whether symptomatic or asymptomatic,
  • with changes in the level of consciousness and cognition that may interfere with the assessment,
  • use of metal implants,
  • pacemakers and implantable cardioverter (ICD),
  • those who presented postoperative complications such as infection in the sternotomy

结局指标

主要结局

respiratory muscle strength

时间窗: through study completion, an average of 1 year

measured in centimeters of water

cough peak flow

时间窗: through study completion, an average of 1 year

measured in liters per minute

slow vital capacity

时间窗: through study completion, an average of 1 year

measured in milliliters per kilo

次要结局

  • painful sensation(through study completion, an average of 1 year)
  • length of stay(through study completion, an average of 1 year)
  • cardiac variability(through study completion, an average of 1 year)

研究者

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

Max de Araujo Melo

Principal Investigator

Universidade Federal de Pernambuco

研究点 (2)

Loading locations...

相似试验