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临床试验/NCT02694991
NCT02694991已完成4 期

Osteopathic Manipulative Treatment Efficacy in Sternal Pain Management After Heart Surgery

Fondazione Don Carlo Gnocchi Onlus2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2013年9月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
80
试验地点
2
主要终点
Pain intensity relief

研究概览

简要总结

Effectively controlling sternal pain during cardiac rehabilitation after heart surgery is very important as it reduces the risk of postoperative complications.

However, the contraindications and side effects of analgesic drugs may induce physicians to use them so cautiously that pain may actually be under-treated.

The aim of this open label, controlled study is to assess whether osteopathic manipulative treatment (OMT) can contribute to pain relief and improve rehabilitation outcomes.

详细描述

The currently predominant means of controlling postoperative pain is the peri-operative administration of opioid or non-opioid (acetaminophen) analgesics, alone or in combination, and non-steroidal anti-inflammatory drugs (NSAIDs). However, anti-inflammatory drugs are contraindicated for many patients because they may impair renal function, interact with platelet aggregation, and increase the risk of gastrointestinal damage and bleeding. The spectrum of available options is narrow.

Osteopathic manipulative Treatment (OMT) intervenes in the process that transforms nociceptive information into the subjective experience and it may be useful.

It has been found to be effective in controlling pain after abdominal surgery, it has a beneficial effect on patients recovering coronary artery by-pass surgery and also improves cardiac function The aim of this study was to assess whether complementary OMT is an effective means of reducing post-surgical sternal pain and improving rib cage mobility after heart surgery involving sternotomy, and to investigate its advantages during in-patient rehabilitation in terms of functional recovery, and perceived anxiety and depression.

This open, randomised, semi-blinded, controlled trial involves inclusion of 80 adult patients of both genders consecutively admitted as in-patients to cardiac rehabilitation unit after undergoing elective coronary artery by-pass grafting (CABG), valve replacement or repair and/or ascending aorta surgery with sternotomy, and capable of voluntarily providing their written informed consent. The patients are divided in 2 groups, the intervention group receiving OMT and the control group. Both groups are following the same rehabilitation programme and receiving usual care.

All of the subjects taking part in the study are receiving standard care in accordance with the international guidelines for in-patient cardiac rehabilitation; the only experimental intervention is the addition of OMT

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
None

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

  • Recent artery bypass grafting (CABG)
  • Recent valve replacement or repair
  • Recent ascending aorta surgery

排除标准

  • Heart surgery using mini-thoracotomy.
  • Heart transplantation
  • Implant of a ventricular assistance device
  • Diabetes mellitus
  • Rheumatoid arthritis
  • Autoimmune diseases
  • Altered cognitive capacities

结局指标

主要结局

Pain intensity relief

时间窗: 21 days

Pain intensity measured with visual analogic scale (VAS)

次要结局

  • Respiratory function(21 days)
  • Anxiety and Depression(21 days)
  • Functional capacity improvement(21 days)
  • Analgesic drug consumption.(21 days)
  • Hospitalization length(21 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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