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Feasibility and Safety of SEEKflex catheter in Awake Tracheal Intubation for Critically Ill Patients: A Single-Center, Randomized Controlled Clinical Trial

Feasibility and Safety of SEEKflex catheter in Awake Tracheal Intubation for Critically Ill Patients: A Single-Center, Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102248
Enrollment
Unknown
Registered
2025-05-12
Start date
2025-05-15
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Acute respiratory failure (oxygenation index less than 300mmHg)

Interventions

Traditional Group:General catheter guided endotracheal intubation group
SEEK Group:SEEKflex catheter guided endotracheal intubation group

Sponsors

Huai'an First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-85 years. 2. Patients with acute respiratory failure (oxygenation index less than 300mmHg) undergoing awake tracheal intubation for mechanical ventilation. 3. Obtained informed consent and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women. 2. Patients with severe heart disease. 3. Presence of acute pharyngitis or laryngeal edema. 4. Currently participating in other drug clinical trials or participating in other clinical trials within 30 days.

Design outcomes

Primary

MeasureTime frame
One time intubation success rate;

Secondary

MeasureTime frame
Total intubation time;Delirium occurrence;Complications;One time intubation success rate;

Countries

China

Contacts

Public ContactHuang Ying

Huai'an First People's Hospital

huangying5249@163.com+86 517 85801687

Outcome results

None listed

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