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Study of fiberoptic bronchoscope-guided intubation through the left and right nostrils in the treatment of dental caries in children

Study of fiberoptic bronchoscope-guided intubation through the left and right nostrils in the treatment of dental caries in children

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078500
Enrollment
Unknown
Registered
2023-12-11
Start date
2023-12-11
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Dental caries, pulpitis

Interventions

left nostril:After selecting the left nostril and using glycerin to lubricate the fiberoptic bronchoscope core and the tracheal tube, thefiberoptic bronchoscope core is passed through the tracheal tub
right nostril:After selecting the right nostril and using glycerin to lubricate the fiberoptic bronchoscope core and the tracheal tube, the fiberoptic bronchoscope core is passed through the tracheal

Sponsors

Anhui Provincial Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 6 Years

Inclusion criteria

Inclusion criteria: 1, gender is not limited, age 3-6 years old, 2, ASA classification ?-?, 3, elective caries treatment surgery, 4, after fully explaining the content of the clinical trial, the child's family voluntarily subjected to the trial and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1, children with anatomical deformities of the nasal cavity such as deviated septum and septal bony spurs as well as enlarged turbinates, children with recurrent rhinorrhea, nasal polyposis, and risk of gastroesophageal reflux, 2, children with previous palatoplasty, cyanotic cardiac disease, chronic sinusitis, abnormal coagulation status, last week's use of anti-inflammatory medications, or a difficult or potentially difficult airway, 3, preoperative asthma, epilepsy, and cardiac insufficiency, and 4, children judged to be of a family that lacks the capacity to give consent.

Design outcomes

Primary

MeasureTime frame
Intubation time;

Secondary

MeasureTime frame
nosebleed;

Countries

China

Contacts

Public ContactYue Kun

Anhui Provincial Children's Hospital

kuncl_0018@163.com+86 152 5515 5050

Outcome results

None listed

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