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Airway ManagementNCT07574450

Taiwan ED Airway Quality Surveillance Registry (TEAR)

An observational study of Airway Management and Tracheal Intubation, run by Chang Gung Memorial Hospital at 1 site in Taiwan.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This prospective, multicenter observational registry systematically captures all emergency department tracheal intubations across participating hospitals in Taiwan. The registry focuses on process quality indicators, including first-pass success, and patient-safety outcomes, including hypoxemia, hypotension, and… Read more about this study

Who is it for?
Ages 18 years and older
How many people
1,200 participants
Where
1 siteTaiwan
Study dates
Aug 2026to Dec 2029
How long will I take part?
1 Month
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Consecutive adult emergency department patients undergoing tracheal intubation at participating hospitals in Taiwan.

Who may be able to join

  • Undergoing tracheal intubation in the emergency department during the study period

Who cannot join

  • Prehospital intubation; intubation performed solely for elective anesthesia/procedural sedation outside emergency indications

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

TING HAO YANG, Doctor contact

+886978989007

mr2434@cgmh.org.tw

Taiwan1 site
  • New Taipei Municipal Tucheng Hospital, New Taipei City, Taiwan

    New Taipei City

    TING HAO YANG, Doctor, +886978989007, mr2434@cgmh.org.tw

Other trials in Taiwan

About this study

Official title: The Taiwan ED Airway Quality Surveillance Registry (TEAR): A Prospective Multicenter Observational Study

This prospective, multicenter observational registry systematically captures all emergency department tracheal intubations across participating hospitals in Taiwan. The registry focuses on process quality indicators, including first-pass success, and patient-safety outcomes, including hypoxemia, hypotension, and peri-intubation cardiac arrest within 30 minutes of intubation. Routinely generated laboratory and physiologic variables are also collected to improve risk stratification and identify predictors of major adverse events. The study is non-interventional and does not alter clinical care.

Keywords
first-pass success, hypoxemia, hypotension, cardiac arrest, registry
Medical subject headings
Emergencies, Hypoxia, Hypotension, Heart Arrest

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07574450
Study groupRoleWhat they receive
Adult patients in ED require emergent tracheal intubationNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of major adverse peri-intubation events within 30 minutes after the start of intubation

    severe hypoxemia, severe hypotension/cardiovascular instability, or cardiac arrest.

    Measured: Periprocedural, through 30 minutes after the start of intubation

Secondary outcomes (2)
  1. First-pass success

    Measured: Periprocedural

  2. In-hospital mortality

    Measured: From intubation to hospital discharge, assessed up to 90 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 May 2026
  2. Study startAug 2026 (estimated)
  3. Primary completionJul 2029 (estimated)
  4. Study completionDec 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,200 participants (estimated)
Target duration
1 Month
IDs, dates and publications
ClinicalTrials.gov ID
NCT07574450
Sponsor's protocol ID
202501836B0
Status last verified
May 2026
First submitted
27 Apr 2026
Last updated
8 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: De-identified data will be retained under institutional governance and are not currently planned for public individual participant data sharing.

Publications

  • Garcia SI, Smischney NJ, Sandefur BJ, D'Andria Ursoleo J, Kelm DJ, Wieruszewski PM. Peri-intubation Cardiovascular Collapse During Emergency Airway Management. Pulm Ther. 2025 Dec;11(4):569-585. doi: 10.1007/s41030-025-00326-x. Epub 2025 Oct 16.

    PubMed 41094343
  • Hasegawa K, Hagiwara Y, Chiba T, Watase H, Walls RM, Brown DF, Brown CA 3rd; Japanese Emergency Medicine Research Alliance. Emergency airway management in Japan: Interim analysis of a multi-center prospective observational study. Resuscitation. 2012 Apr;83(4):428-33. doi: 10.1016/j.resuscitation.2011.11.027. Epub 2011 Dec 8.

    PubMed 22155701
  • Maia IWA, Besen BAMP, Silva LOJE, von Hellmann R, Hajjar LA, Sandefur BJ, Pedrollo DF, Nogueira CG, Figueiredo NMP, Miranda CH, Martins D, Baumgratz TD, Bergesch B, Costa D, Colleoni O, Zanettini J, Freitas AP, Moreira NP, Gaspar PL, Tambelli R, Costa MC, Silveira S, Correia W, de Maria RG, Filho UAV, Weber AP, da Silva Castro V, Dornelles CFD, Tabach BS, Guimaraes HP, Stanzani G, Gava TF, Mullan A, Souza HP, Ranzani OT, Bellolio F, Alencar JCG; BARCO group. Peri-intubation adverse events and clinical outcomes in emergency department patients: the BARCO study. Crit Care. 2025 Apr 17;29(1):155. doi: 10.1186/s13054-025-05392-w.

    PubMed 40247381
  • Cho J, Cho YS, You JS, Lee HS, Kim H, Chung HS; Korean Emergency Airway Management Society. Current status of emergency airway management for elderly patients in Korea: Multicentre study using the Korean Emergency Airway Management Registry. Emerg Med Australas. 2013 Oct;25(5):439-44. doi: 10.1111/1742-6723.12122. Epub 2013 Sep 9.

    PubMed 24099373
  • April MD, Arana A, Reynolds JC, Carlson JN, Davis WT, Schauer SG, Oliver JJ, Summers SM, Long B, Walls RM, Brown CA 3rd; NEAR Investigators. Peri-intubation cardiac arrest in the Emergency Department: A National Emergency Airway Registry (NEAR) study. Resuscitation. 2021 May;162:403-411. doi: 10.1016/j.resuscitation.2021.02.039. Epub 2021 Mar 5.

    PubMed 33684505
  • Alkhouri H, Vassiliadis J, Murray M, Mackenzie J, Tzannes A, McCarthy S, Fogg T. Emergency airway management in Australian and New Zealand emergency departments: A multicentre descriptive study of 3710 emergency intubations. Emerg Med Australas. 2017 Oct;29(5):499-508. doi: 10.1111/1742-6723.12815. Epub 2017 Jun 5.

    PubMed 28582801
  • Russotto V, Myatra SN, Laffey JG, Tassistro E, Antolini L, Bauer P, Lascarrou JB, Szuldrzynski K, Camporota L, Pelosi P, Sorbello M, Higgs A, Greif R, Putensen C, Agvald-Ohman C, Chalkias A, Bokums K, Brewster D, Rossi E, Fumagalli R, Pesenti A, Foti G, Bellani G; INTUBE Study Investigators. Intubation Practices and Adverse Peri-intubation Events in Critically Ill Patients From 29 Countries. JAMA. 2021 Mar 23;325(12):1164-1172. doi: 10.1001/jama.2021.1727.

    PubMed 33755076

Questions about this trial

What is this clinical trial studying?

An observational study of Airway Management and Tracheal Intubation, run by Chang Gung Memorial Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 8 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact TING HAO YANG, Doctor (+886978989007, mr2434@cgmh.org.tw), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of major adverse peri-intubation events within 30 minutes after the start of intubation (time frame: Periprocedural, through 30 minutes after the start of intubation). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07574450, which also lists 7 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 May 2026.

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