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临床试验/NCT07183670
NCT07183670Enrolling By Invitation不适用

Application of a Voice Valve-Based Decannulation Protocol in Tracheostomized Patients With a Prolonged Disorders of Consciousness: A Prospective Multicenter Cohort Study

Hongying Jiang, MD2 个研究点 分布在 1 个国家目标入组 184 人开始时间: 2026年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
184
试验地点
2
主要终点
Decannulation success rate

研究概览

简要总结

To evaluate the feasibility of a standardized tracheostomy decannulation protocol for patients with prolonged Disorders of Consciousness (pDoC) in rehabilitation hospitals.

详细描述

Advances in critical care have significantly increased the number of survivors with severe acquired brain injury (sABI). A subset of these patients develops Disorders of Consciousness (DoC), defined as prolonged DoC (pDoC) when lasting >28 days. Tracheostomy is often indicated for long-term mechanical ventilation and airway protection. However, tracheostomy tubes may cause inflammation, stenosis, excessive coughing, and dysphagia. Decannulation improves patient comfort, appearance, swallowing, communication, and social reintegration, while reducing long-term complications (e.g., tracheal stenosis, malacia, vocal cord injury, accidental decannulation) . Despite these benefits, consensus on safety and optimal timing for decannulation in pDoC remains elusive due to uncertain airway protection and aspiration risks. Our center previously demonstrated that a standardized decannulation protocol implemented by a pulmonary rehabilitation team correlates with successful decannulation. Key innovations include: (1) Replacing capping trials with 4-hour continuous tolerance of a speaking valve (reducing airway resistance and delayed decannulation ); (2) Not considering dysphagia a contraindication if patients manage secretions effectively and retain cough strength, even if requiring enteral nutrition (nasogastric/jejunal tubes or PEG) . This multicenter study aims to validate this protocol in pDoC patients and assess changes in consciousness levels pre-/post-decannulation.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Tracheostomy status
  • •The duration of consciousness disorders> 28 days
  • •CRS-R score >0 and <17
  • •Signed informed consent by legal representative

排除标准

  • •Non-PDOC tracheostomy patients
  • •Death within 2 weeks post-referral

研究组 & 干预措施

Decannulation Cohort

Patients who pass decannulation protocol

干预措施: decannulation protocol (Diagnostic Test)

Not-decannulation Cohort

Patients failing at any protocol stage

干预措施: decannulation protocol (Diagnostic Test)

结局指标

主要结局

Decannulation success rate

时间窗: At 48 hours post decannulation

(Decannulation - Decannulation failure ) / Total number of enrolled patients

次要结局

  • Reintubation rate(90days follow-up)
  • Coma Recovery Scale-Revised (CRS-R) scores(through study completion, an average of 1 year)
  • CRS-R change rate(At a week post decannulation)
  • Time to decannulation(through study completion, an average of 1 year)

研究者

发起方
Hongying Jiang, MD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hongying Jiang, MD

Principal Investigator

Capital Medical University

研究点 (2)

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