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临床试验/NCT06891248
NCT06891248尚未招募不适用

The Utility of Osteopathic Manipulative Medicine in Weaning Patients from the Ventilator

Oklahoma State University Center for Health Sciences0 个研究点目标入组 20 人开始时间: 2025年3月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
20
主要终点
Time on ventilator

研究概览

简要总结

The objectives of this research are to determine the treatment effect size of OMM to wean patients off of the ventilator, determine the number of patients needed for a larger study (power), determine the willingness of patients/POAs to be recruited, identify the correct dosing of OMM and whether there are concerns for the safety of treatment, and determine whether the hypothesis is feasible for a larger study. The primary outcome measure is the duration of time until a subject is weaned off of mechanical ventilation using Osteopathic Manipulative Medicine (OMM). The secondary outcome measures (see the next section for further explanation) are to determine if OMM affects changes in morbidity and mortality, such as VBG/ABG, NIF, RSBI, P 0.1, FiO2, PEEP, mental status, hemodynamic stability (blood pressure), spontaneous TV, reintubation after extubation, and death.

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 (Investigator)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Acute respiratory failure (hypoxic, hypercapnic, or neuromuscular)
  • •Not making satisfactory progress with weaning after being on the ventilator for more than 48 hours
  • •Clinical stability for pressure support trial with ventilator to monitor ventilation progression
  • •Pulmonology must be following the patient for standardized ventilator management approach and interventions as needed
  • •Medical power of attorney (POA) or legally authorized representative (LAR) who is able to consent subject for trial enrollment and treatment
  • •Patients who were not referred to the OMM service

排除标准

  • •Age less than 18 years old or more than 85 years old
  • •Moderate/severe neurological disease with expectation of non-progression off the ventilator or poor quality of life predicted (including end-stage dementia with the expectation of non-progression off ventilator, multiple sclerosis, ALS, anoxic brain injury, etc)
  • •Status epilepticus or EEG result pending
  • •Post-arrest hypothermia protocol
  • •Acute stroke
  • •Acute rib fractures preventing the implementation of the treatment protocol
  • •Acute spinal injury preventing the implementation of the treatment protocol
  • •Recent head injury requiring close clinical monitoring
  • •Ejection Fraction less than 15%
  • •Pleural effusion requiring procedural intervention or inhibiting ventilator progress
  • •Pericardial effusion or tamponade requiring procedural intervention or inhibiting ventilator progress
  • •ACLS/cardiac arrest within the past 72 hours
  • •Confirmed opioid overdose with positive urine drug screen and response to naloxone
  • •Patients who were referred to the OMM service

研究组 & 干预措施

Control

No Intervention

Subjects in these arms only receive conventional care

Osteopathic Manipulative Treatment

Experimental

The standard OMM treatment arm includes a 10-minute treatment time for 5 body regions with up to 3 providers working on the patient simultaneously. The OMM attending physician will be physically present and supervising the treatment, and may be participating in the treatment. The 5 body regions include Head, Neck, Thoracic, Ribs, and Abdominal/Diaphragm. The standard technique for the OMM arm includes OA decompression, screening and treating any cervical dysfunction, thoracic inlet myofascial release, rib raising, thoracic paraspinal inhibition, and abdominal diaphragm myofascial release.

There is an opportunity for an additional 5 minutes of treatment time and additional regions if the lead physician determines it is appropriate based on clinical judgment. The additional 4 regions include Upper Extremity, Lower Extremity, Lumbar, Pelvis, and Sacrum.

干预措施: Osteopathic Manipulative Treatment (Procedure)

结局指标

主要结局

Time on ventilator

时间窗: 90 days

Number of days that the patient is on the ventilator after inclusion in the study

次要结局

  • Ventilator associated measurement(90 days)
  • Blood pressure(90 days)
  • Mental status(90 days)
  • Reintubation(90 days)
  • Mortality(90 days)

研究者

发起方
Oklahoma State University Center for Health Sciences
申办方类型
Other
责任方
Principal Investigator
主要研究者

Leslie Ching

Clinical Associate Professor

Oklahoma State University Center for Health Sciences

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