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The Impact of Tracheostomy Timing on Postoperative Pulmonary Complications in Stroke Patients

The Impact of Tracheostomy Timing on Postoperative Pulmonary Complications in Stroke Patients - TTPS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091423
Enrollment
Unknown
Registered
2024-10-28
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

study group:Tracheostomy performed within 72 hours after intubation
control group:Tracheostomy performed more than 72 hours after intubation.

Sponsors

The Second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) ICU stroke patients in a coma after decompressive surgery (GCS < 9) 2) Diagnosis of one of the following: a. Non-traumatic acute ischemic stroke (AIS) b. Non-traumatic intracerebral hemorrhage (ICH) c. Non-traumatic subarachnoid hemorrhage (SAH) 3) Legal representative signs the informed consent form 4) Major indications for tracheostomy (at least one of the following): a. Frequent need for suctioning b. Central nervous system-related respiratory insufficiency c. Aspiration or risk of aspiration due to dysphagia 5) Endotracheal intubation with mechanical ventilation 6) Age = 18 years.

Exclusion criteria

Exclusion criteria: 1) Severe underlying respiratory disease: severe obstructive pulmonary disease 2) Pregnancy 3) Stroke involving the respiratory center (e.g., brainstem hemorrhage leading to abnormal respiratory rhythm or rate) 4) Contraindications to tracheostomy 5) BMI = 35 kg/m² 6) Informed consent not signed 7) Intubation with mechanical ventilation for more than 3 days 8) Existing or anticipated life-threatening emergency prior to tracheostomy 9) Family unwilling to continue aggressive treatment for 3 weeks, potentially leading to treatment withdrawal

Design outcomes

Primary

MeasureTime frame
Postoperative pulmonary complication rate;

Secondary

MeasureTime frame
Ventilator free days at 28 days;28-day mortality;In-hospital mortality;Length of hospital stay;Length of ICU stay;

Countries

China

Contacts

Public ContactYun Sun

The Second Affiliated Hospital of Anhui Medical University

sunyun9653@126.com+86 130 8340 0880

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026