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Application of nasopharyngeal airway to painless enteroscopy in patients with potentially difficult airway

Application of nasopharyngeal airway to painless enteroscopy in patients with potentially difficult airway

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103967
Enrollment
Unknown
Registered
2025-06-09
Start date
2025-01-04
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Upper airway obstruction

Interventions

Control group:Routine oxygen airway management (without prior NA)
Intervention group:A nasopharyngeal vent tube was used in advance to assist airway management.

Sponsors

Cancer Hospital, Chongqing University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Adult patients aged 18-75 years. 2.Patients scheduled to undergo a painless colonoscopy. 3.Patients with potentially difficult airway characteristics indicated by preoperative evaluation (patients with potentially difficult airway characteristics indicated by pre-examination evaluation (Wilson score =2 May have difficult airway; Wilson risk Score was used as a scoring tool to predict difficult tracheal intubation. Wilson risk score mainly included five indicators: 1 score for body weight of 90-110kg and 2 score for body weight > 110kg; Head and neck motion about 90° is 1 min, <90° is 2 min; Mouth opening degree 5cm is 1 point, <5cm is 2 points; The degree of mandibular retraction was 1 point in medium and 2 points in severe. The ability of incisor protrusion was 1 point in medium and 2 points in severe).

Exclusion criteria

Exclusion criteria: 1.Patients with oropharyngeal structural abnormalities or severe oral infections; 2.People with a known history of allergies or allergies to OPA materials; 3.Patients who have had upper respiratory tract surgery recently (within 3 months). 4.Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Incidence of intraoperative hypoxia (SpO2<90%);

Secondary

MeasureTime frame
Operator satisfaction score;Intraoperative incidence of clinical respiratory depression (SpO2 of 90%-95%) and severe hypoxia (SpO2 of 75%-89% with a duration greater than 60 s or SpO2<75%);Usage of hypoxic event handling measures;Entry time;The success rate of reaching the blind;Incidence of intraoperative and postoperative adverse reactions;Airway management success rate;Detection rate of adenoma;

Countries

China

Contacts

Public ContactJuan Jiang

Cancer Hospital, Chongqing University

13452081013@163.com+86 13452081013

Outcome results

None listed

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