Skip to content

Effectiveness of SEEKflex assisted nasotracheal intubation:a multicenter randomized controlled clinical trial

Effectiveness of SEEKflex assisted nasotracheal intubation:a multicenter randomized controlled clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086738
Enrollment
Unknown
Registered
2024-07-09
Start date
2024-07-15
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

None

Interventions

SEEKflex Group:Nasal tracheal intubation was performed using SEEKflex guidance
Routine Group:Nasal tracheal intubation was performed using conventional methods

Sponsors

Shanghai Pudong New Area People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.ASA grade I-III 2. Age: 8-80 years old 3. Patients requiring general anesthesia through nasal tracheal intubation

Exclusion criteria

Exclusion criteria: 1. Emergency surgery 2. Pathological changes of oropharyngeal area 3. Coagulation dysfunction 4. Difficulty in expected mask ventilation 5. Get pregnant 6. Refused to participate in this clinical study

Design outcomes

Primary

MeasureTime frame
Incidence of nosebleed in 90s after intubation;

Secondary

MeasureTime frame
Nasopharyngeal bleeding 5 minutes after intubation;Number of intubation attempts (success rate per intubation);Total intubation time (from laryngoscope insertion to tracheal catheter entry into glottis);Whether auxiliary intubation is required;Duration and frequency of patients with low oxygen saturation (SpO2<90%);Esophageal insertion or not and the number of times;Whether the intubation technique needs to be replaced;Loosening or loss of teeth due to intubation;

Countries

China

Contacts

Public ContactXia Jianhua

Shanghai Pudong New Area People's Hospital

jianhuaxia2000@sina.com+86 136 0180 2789

Outcome results

None listed

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