The Effect of Different Fiberoptic Outer Diameters on Fiberoptic Intubation
NCT ID: NCT06709118
Last Updated: 2024-11-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
75 participants
OBSERVATIONAL
2024-12-10
2025-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
In clinical work, it was found that the tracheal catheter was easily blocked when it passed through the glottis, and it was necessary to adjust the position of the tracheal catheter for several times before the tracheal catheter could be sent into the tracheal tube, which was easy to cause throat injury in the process. At present, relevant studies are mainly focused on the first step of bronchoscopic intubation, how to quickly expose the glottis and complete the bronchoscopic guidance process. However, there is no clear mention of the situation of catatoning in the process of endotracheal catheter and how to solve the problem of catatoning.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
3.8mm Group
Orotracheal intubation was performed with a 3.8 millimeter outer diameter fiberoptic
fiberoptic
Tracheal intubation was performed with different outer diameters of fiberoptic.
2.8 mm group
Orotracheal intubation was performed with a 2.8 millimeter outer diameter fiberoptic
fiberoptic
Tracheal intubation was performed with different outer diameters of fiberoptic.
4.8mm group
Orotracheal intubation was performed with a 4.8 millimeter outer diameter fiberoptic
fiberoptic
Tracheal intubation was performed with different outer diameters of fiberoptic.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
fiberoptic
Tracheal intubation was performed with different outer diameters of fiberoptic.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2.18-60 year
3.Adult patients requiring general anesthesia for orotracheal intubation
Exclusion Criteria
2. limited movement of temporomandibular joint
3. abnormal glottic anatomy
4. polyps of vocal cords
18 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Qinye Shi
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Qinye Shi
The Fourth Affiliated Hospital of Zhejiang University Medical College
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
References
Explore related publications, articles, or registry entries linked to this study.
Piegeler T, Clausen NG, Weiss M. Effectiveness of tip rotation in fibreoptic bronchoscopy under different experimental conditions: an in vitro crossover study. Br J Anaesth. 2017 Dec 1;119(6):1206-1212. doi: 10.1093/bja/aex322.
Karmali S, Rose P. Tracheal tube size in adults undergoing elective surgery - a narrative review. Anaesthesia. 2020 Nov;75(11):1529-1539. doi: 10.1111/anae.15041. Epub 2020 May 16.
Teulieres M, Berard E, Marot V, Reina N, Ferre F, Minville V, Cavaignac E. A quadruple peripheral nerve block outside the OR for anterior cruciate ligament reconstruction reduces the OR occupancy time. Knee Surg Sports Traumatol Arthrosc. 2023 Jul;31(7):2917-2926. doi: 10.1007/s00167-022-07246-2. Epub 2022 Dec 5.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
KY-2024-172
Identifier Type: -
Identifier Source: org_study_id