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Efficacy and safety of esticketamine combined with Ultra-slippery endotracheal catheter for reducing airway injury during endotracheal intubation: a randomized controlled multicenter study

Efficacy and safety of esticketamine combined with Ultra-slippery endotracheal catheter for reducing airway injury during endotracheal intubation: a randomized controlled multicenter study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060807
Enrollment
Unknown
Registered
2022-06-12
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

Trachea intubation airway injury

Interventions

Experimental group:Ultra-slippery Anti-adhesion coating material for tracheal tube
The control group:Conventional tracheal tube

Sponsors

Guangzhou Women and Children's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 6 Years

Inclusion criteria

Inclusion criteria: 1. An elective operation through airway intubation under general anesthesia is planned; 2. ASA score level 1-2; 3. Informed consent signed by the patient and legal representative.

Exclusion criteria

Exclusion criteria: 1. Neck, throat or oropharynx surgery is planned; 2. oropharynx or neck deformity; 3. Previous history of endotracheal intubation or tracheotomy; 4. Wheezing or phonation disorders; 5. Patients requiring nasogastric tube or orogastric tube; 6. Situations that other researchers deem inappropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
The incidence of pharyngeal pain 8 hours after extubation;—

Countries

China

Contacts

Public ContactBaisong Zhao

Guangzhou Women and Children's Medical Center

zhaobaisong819@163.com+86 13642665097

Outcome results

None listed

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