Critical IllnessCHECCNCT06791317
Intubation Checklist in the Intensive Care Unit
An observational study of Critical Illness and Respiratory Failure, run by Karolinska University Hospital at 1 site in Sweden.
Trial summary
This retrospective study aims to explore whether the introduction of a preprocedural checklist for intubation in the intensive care unit (ICU) is associated with a lower incidence of intubation-related complications. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Critical Illness, Respiratory Failure, Unconsciousness
- What is being tested?
- Checklist
- How many people
- 60 participants
- Where
- 1 siteSweden
- Study dates
- 15 Jan 2025to 15 May 2025
- How long will I take part?
- 3 Months
- Phase
- Observational
- Are there results?
- None posted in the registry
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: Intensive Care Patients that undergo tracheal intubation. All patients (before and after checklist) are registered with a protocol during intubation. This protocol is registered in a Respiratory Database.
Who may be able to join
- Patient in the ICU
- Need for tracheal intubation
Who cannot join
- Pateint is under 18 years of age
- Patiend inclusion is decided not suitable for any reason by the intensivist
Trial locations and contacts
1 site in 1 country.
Sweden1 site
Karolinska University Hospital, Perioperative Medicine and Intensive Care
Stockholm, 17176
About this study
Official title: Does Checklist Utilisation Decrease Complications Related to Intubation of the Critically Ill Adult? - a Two-phase Retrospective Study
This retrospective study aims to explore whether the introduction of a preprocedural checklist for intubation in the intensive care unit (ICU) is associated with a lower incidence of intubation-related complications. Using a database where protocols from intubations in the ICU before implementing a checklist and after we will investigate whether a checklist affects early desaturation and hypotension after intubation.
Read the detailed description
PROJECT PLAN
Does checklist utilisation decrease complications related to intubation of the critically ill adult? - a two-phase study
Study code: CHECC (Checklist for Endotracheal intubation in the Critical Care)
Ethical approval: This study will be conducted in accordance with GCP and National Swedish standards, as well as local standard procedures at the Clinical Research Unit at Function Perioperative Medicine and Intensive Care, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Principal investigator: Jessica Kåhlin, MD, PhD
Investigators:
Atosa Nejatian, MD Ida-Maria Forsberg, MD, PhD Malin Jonsson Fagerlund, MD, Assoc Professor
Affiliations for the above:
Perioperative Medicine and Intensive Care (PMI), Karolinska University Hospital and Department of Physiology and Pharmacology, Section for Anesthesiology and Intensive Care Medicine, Karolinska Institutet, Stockholm, Sweden
Background Endotracheal intubation is one of the most frequently performed procedures in the intensive care setting. However, it is associated with an alarmingly high incidence of complications. A recent study of emergency intubations performed in the intensive care unit (ICU), emergency department and wards found that approximately 40% resulted in intubation-related major adverse events, more commonly hypotension and hypoxemia. In addition, cardiac arrest was seen in 3% of intubations. These findings suggest that although endotracheal intubation is a common procedure, it still present a significant hazardous risk for the patient.
Preprocedural checklists have been used and implemented in various aspects and settings of health care. Among others, implementing a surgical checklist resulted in lower morbidity and mortality and in the ICU, using a checklist in conjunction with the placement of a central venous line significantly reduced central line-associated bloodstream infections.
A study on implementing a preprocedural intubation checklist on trauma patients in the emergency department showed a reduction in intubation-related complications such as oxygen desaturation, hypotension.
Checklists are a cognitive aid and practical tool to help planning and optimising a procedure systematically and set order. They promote standardisation and reduce reliance on individual memory, which can be compromised by stress and fatigue. This is used in aviation, product management and different healthcare areas. It usually contains a list of required items or suggestions and serves as a reminder how to optimise the patient, preferably with a contingency plan. Hence, in theory, this makes endotracheal intubation an ideal procedure for applying the checklist in critical ill patients in the ICU.
Intubation of the critically ill adult is associated with a significant risk of major complications, with patients having a limited physiological reserve, presenting a unique challenge for the intensivist. Guidelines advocate the employment of structured checklists for intubation. Preprocedural checklists have been used and significantly improved patient care in other aspects of health care. However, the number of studies on intubation checklists in the intensive care setting is currently limited, with contradictory results.
Therefore, we aim to investigate whether implementing a preprocedural intubation checklist in the ICU reduces in intubation-related complications in critically ill adults.
Objectives and purpose
This study aims to explore whether the introduction of a preprocedural checklist for intubation in the intensive care unit is associated with a lower incidence of intubation-related complications. The researchers hypothesise that the introduction and utilisation of a checklist will contribute to a safer and more structured working climate, leading to an optimised surrounding environment and enhanced physiology of the patient.
Research question
The primary hypothesis is that implementing a checklist for intubation in the intensive care will reduce hypoxemic and hypotensive events. The secondary hypothesis is that a checklist will reduce other adverse events, such as severe arrhythmias or fatal outcomes.
Primary endpoint:
Intubation-related complications:
- Peripheral oxygen saturation (SpO2) below 90% (or >5% drop if saturation is <90% after preoxygenation).
- Hypotension with systolic arterial blood pressure below 90 mmHg.
Secondary endpoints:
Does the implementation of a checklist for intubation result in the following:
- Decreased: 30-day mortality, ventilator days, ventilator-associated pneumonia, days in the ICU?
- A decreased number of intubation attempts and a higher first-pass success rate?
- A higher lowest median SpO2 from induction of anaesthesia until up to 5 min after intubation?
- A lower frequency of severe complications (severe arrhythmias, cardiac arrest, death)?
- A lower rate of intubation-related difficulties (change of method, change of operator, oesophageal intubation)?
- Decrease the duration of intubation (from laryngoscopy until end-tidal CO2 is registered)?
- Perceived difficulties, advantages and operator stress?
Design of study
This is and observational two-phase study, with the introduction of a checklist prior to phase two. The first phase will consist of a period of 6 to 8 months, and data regarding these intubations will be collected from the pre-existing quality register at the ICU. After this period, a checklist for intubation will be introduced and implemented, and endotracheal intubation will commence with the walkthrough of this cognitive aid. After the introduction of the checklist, the second phase of the study is started, where protocols on intubation will be collected and compared to the data from the first period.
Inclusion criteria
- Adult, ≥18 years old
- Intensive care patient that requires tracheal intubation for any indication
Exclusion criteria
- Decided not suitable for any reason by the intensivist.
- Under 18 years of age
If the checklist, for any reason, is not used for a patient after the implementation period, the data will still be included in the group of the second phase, since we believe the ICU staff will be considerably exposed to the checklist and hence, influenced by it.
Description of project This observational retrospective study will be conducted in the ICU, Karolinska University Hospital, Solna. The aim is to study whether introducing and implementing a pre-intubation checklist are associated with a lower incidence of intubation-related adverse events.
Adult ICU patients requiring intubation for any indication will be included, with inclusion and exclusion criteria as described above.
In a quality registry of ICU intubations, parameters such as pulse, blood pressure and SpO2 prior to, during and up to 5 minutes after intubation are manually registered from the monitor and put into the "ICU Respiration database". In addition, other intubation-related information is also registered, for instance: duration of intubation, airway assessment, intubation difficulty scale, intubation method and equipment, preoxygenation and intubation-related complications.
The study will consist of two phases. During the second phase, a checklist will be introduced and implemented based on the review of ICU airway guidelines and available literature. Physicians, residents and ICU nurses will receive information regarding the checklist prior to the intervention phase. If the checklist is not used for a patient during the second phase, the data will still be used in the cohort of the second group.
Data will be collected using the same intubation protocol as before the checklist introduction, containing patient demographics, the reason for ICU admission and intubation and vital parameters (saturation, blood pressure, pulse) before, during and after intubation. Blood gas analysis for arterial oxygen and carbon dioxide partial pressure will be analysed prior to intubation and in the immediate period after intubation (clinical practice). Furthermore, outcomes that will be registered are immediate complications such as desaturation, arterial hypotension, severe cardiac arrhythmia, cardiac arrest, death, oesophageal intubation, regurgitation, or a need for a surgical airway. Information regarding preoxygenation method, intubation circumstances and vasopressor use will be gathered, as well as 30-day mortality, length of hospital stay and ventilator days. Scores for physiological compromise ( and length of intensive care prior to intubation will be noted. Intubation-related data include the number of intubation attempts, Cormack-Lehane grade, time to end-tidal CO₂, the experience of the intubating physician, intubation difficulty scale, need for an alternative airway management and change of operator.
In both groups, the duration and method for preoxygenation and the drugs for anaesthetic induction are chosen as appropriate by the responsible intensivist.
Data will be collected from Clinisoft, the intensive care patient chart, regarding all intubations during the study period to find how many patients out of the total cohort that is not included during the study period.
The primary outcome is a comparison of intubation-related hypoxemic and hypotensive events between the two groups. Secondary events as severe arrhythmias, cardiac arrest, fatality and the number of intubation attempts will be analysed.
Statistics Data will be expressed as mean ± SD, median and range, 95% confidence intervals or number and percentage as appropriate. Comparison of two proportions will be performed using the chi-square test or Fischer exact test, where appropriate. Comparison of means will be performed using the student's t-test, while the comparison of medians will be analysed with the Mann-Whitney test. A p-value of <0.05 will be considered significant. Since this is a two-phase observational study of implementing a quality enhancing tool, it is, therefore, impossible to perform a correct power calculation. All the data, as mentioned above, will be compared between the two groups.
Clinical relevance Endotracheal intubation entails a significant risk of life-threatening complications in the intensive care setting. Therefore, optimising this procedure is of utmost importance. We aim to study whether the introducing and implementing a structured checklist for intubation will increase the safety of this standard yet perilous procedure. This could reduce the incidence of severe intubation-related complications and greatly benefit ICU patients.
- Conditions
- Critical Illness, Respiratory Failure, Unconsciousness
- Being tested
- Checklist
- Medical subject headings
- Critical Illness, Respiratory Insufficiency, Unconsciousness
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ChecklistOther
A checklist for the intubation procedure was organised into the categories physiological optimisation, equipment and drugs, team line-up, and contingency plan. This checklist was implemented in the clinic.
| Study group | Role | What they receive |
|---|---|---|
| Standard care | Intubation procedure before introduction of a checklist Receives: Other: Checklist | |
| Checklist group | Intubation procedure after introduction of a checklist Receives: Other: Checklist |
What is being measured
The primary outcome is the main question the study is designed to answer.
Level of desaturation
- Peripheral oxygen saturation (SpO2) below 90% (or >5% drop if saturation is <90% after preoxygenation).
Measured: From intubation up to 5 minutes after the procedure
Level of lowering blood pressure
A systolic arterial pressure (SAP) below 90 mmHg
Measured: From intubation up to 5 minutes after the procedure
Secondary outcomes (11)
30-day mortality
Measured: 30 days
Ventilator days
Amount of days on the ventilator in the intensive care unit
Measured: 30 days
Days in the intensive care unit
A number describing the length of stay for the patient in the intensive care unit
Measured: 3 months
Number of intubation attempts
This describes how many attempts the anesthesiologist needs to complete intubation
Measured: 1 hour
First-pass success rate
How many intubations succeed on the first try?
Measured: 1 hour
Lowest median oxygen saturation
Lowest median oxygen saturation after intubation
Measured: From induction of anaesthesia until up to 5 min after intubation?
Number of arrythmias
Asystole, bradycardia, takyarrythmia
Measured: Up to 5 min after intubation
Presence of cardiac arrest
Circulatory arrest
Measured: Up to 5 minutes after intubation
Change of intubation method
Does the method of intubation (laryngoscopy with tube, laryngeal device, thracheostomy) need to be abandoned or changed?
Measured: 1 hour
Change of operator during intubation?
New operator due to failure of the first one?
Measured: During intubation
Intubation time
Time from laryngoscopy until end-tidal CO2 is registered
Measured: 5 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Jan 2025
- Study start15 Jan 2025
- Primary completion15 May 2025
- Study completion15 May 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Critical IllnessStudies of the same condition, open and under way.
- More trials run by Karolinska University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Other
- Enrolment
- 60 participants (actual)
- Target duration
- 3 Months
Sponsor and investigators
- Lead sponsor
- Karolinska University Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jessica Kåhlin, Karolinska University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06791317
- Sponsor's protocol ID
- K2023-5312
- Acronym
- CHECC
- Status last verified
- May 2026
- First submitted
- 15 Jan 2025
- Last updated
- 15 May 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Nejatian A, Forsberg IM, Thoro U, Sjoblom A, Kahlin J. Impact of Checklist Implementation on Endotracheal Intubation-Related Complications in Critically Ill Adults-A Retrospective Before and After Study. Acta Anaesthesiol Scand. 2025 Aug;69(7):e70103. doi: 10.1111/aas.70103.
PubMed 40692385
Study at a glance
From the registry record, last updated by the sponsor on 15 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Does Checklist Utilisation Decrease Complications Related to Intubation of the Critically Ill Adult? - a Two-phase Retrospective Study
- ClinicalTrials.gov ID
- NCT06791317
- Acronym / sponsor ID
- CHECC / K2023-5312
- Conditions
- Critical Illness, Respiratory Failure, Unconsciousness
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Karolinska University HospitalUniversity, hospital or other
- Study start
- 15 Jan 2025 (actual)
- Primary completion
- 15 May 2025 (actual)
- Study completion
- 15 May 2025 (actual)
- First posted
- 24 Jan 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This retrospective study aims to explore whether the introduction of a preprocedural checklist for intubation in the intensive care unit (ICU) is associated with a lower incidence of intubation-related complications. Using a database where protocols from intubations in the ICU before implementing a checklist and after we will investigate whether a checklist affects early desaturation and hypotension after intubation.
Detailed description
PROJECT PLAN
Does checklist utilisation decrease complications related to intubation of the critically ill adult? - a two-phase study
Study code: CHECC (Checklist for Endotracheal intubation in the Critical Care)
Ethical approval: This study will be conducted in accordance with GCP and National Swedish standards, as well as local standard procedures at the Clinical Research Unit at Function Perioperative Medicine and Intensive Care, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.
Principal investigator: Jessica Kåhlin, MD, PhD
Investigators:
Atosa Nejatian, MD Ida-Maria Forsberg, MD, PhD Malin Jonsson Fagerlund, MD, Assoc Professor
Affiliations for the above:
Perioperative Medicine and Intensive Care (PMI), Karolinska University Hospital and Department of Physiology and Pharmacology, Section for Anesthesiology and Intensive Care Medicine, Karolinska Institutet, Stockholm, Sweden
Background Endotracheal intubation is one of the most frequently performed procedures in the intensive care setting. However, it is associated with an alarmingly high incidence of complications. A recent study of emergency intubations performed in the intensive care unit (ICU), emergency department and wards found that approximately 40% resulted in intubation-related major adverse events, more commonly hypotension and hypoxemia. In addition, cardiac arrest was seen in 3% of intubations. These findings suggest that although endotracheal intubation is a common procedure, it still present a significant hazardous risk for the patient.
Preprocedural checklists have been used and implemented in various aspects and settings of health care. Among others, implementing a surgical checklist resulted in lower morbidity and mortality and in the ICU, using a checklist in conjunction with the placement of a central venous line significantly reduced central line-associated bloodstream infections.
A study on implementing a preprocedural intubation checklist on trauma patients in the emergency department showed a reduction in intubation-related complications such as oxygen desaturation, hypotension.
Checklists are a cognitive aid and practical tool to help planning and optimising a procedure systematically and set order. They promote standardisation and reduce reliance on individual memory, which can be compromised by stress and fatigue. This is used in aviation, product management and different healthcare areas. It usually contains a list of required items or suggestions and serves as a reminder how to optimise the patient, preferably with a contingency plan. Hence, in theory, this makes endotracheal intubation an ideal procedure for applying the checklist in critical ill patients in the ICU.
Intubation of the critically ill adult is associated with a significant risk of major complications, with patients having a limited physiological reserve, presenting a unique challenge for the intensivist. Guidelines advocate the employment of structured checklists for intubation. Preprocedural checklists have been used and significantly improved patient care in other aspects of health care. However, the number of studies on intubation checklists in the intensive care setting is currently limited, with contradictory results.
Therefore, we aim to investigate whether implementing a preprocedural intubation checklist in the ICU reduces in intubation-related complications in critically ill adults.
Objectives and purpose
This study aims to explore whether the introduction of a preprocedural checklist for intubation in the intensive care unit is associated with a lower incidence of intubation-related complications. The researchers hypothesise that the introduction and utilisation of a checklist will contribute to a safer and more structured working climate, leading to an optimised surrounding environment and enhanced physiology of the patient.
Research question
The primary hypothesis is that implementing a checklist for intubation in the intensive care will reduce hypoxemic and hypotensive events. The secondary hypothesis is that a checklist will reduce other adverse events, such as severe arrhythmias or fatal outcomes.
Primary endpoint:
Intubation-related complications:
- Peripheral oxygen saturation (SpO2) below 90% (or >5% drop if saturation is <90% after preoxygenation).
- Hypotension with systolic arterial blood pressure below 90 mmHg.
Secondary endpoints:
Does the implementation of a checklist for intubation result in the following:
- Decreased: 30-day mortality, ventilator days, ventilator-associated pneumonia, days in the ICU?
- A decreased number of intubation attempts and a higher first-pass success rate?
- A higher lowest median SpO2 from induction of anaesthesia until up to 5 min after intubation?
- A lower frequency of severe complications (severe arrhythmias, cardiac arrest, death)?
- A lower rate of intubation-related difficulties (change of method, change of operator, oesophageal intubation)?
- Decrease the duration of intubation (from laryngoscopy until end-tidal CO2 is registered)?
- Perceived difficulties, advantages and operator stress?
Design of study
This is and observational two-phase study, with the introduction of a checklist prior to phase two. The first phase will consist of a period of 6 to 8 months, and data regarding these intubations will be collected from the pre-existing quality register at the ICU. After this period, a checklist for intubation will be introduced and implemented, and endotracheal intubation will commence with the walkthrough of this cognitive aid. After the introduction of the checklist, the second phase of the study is started, where protocols on intubation will be collected and compared to the data from the first period.
Inclusion criteria
- Adult, ≥18 years old
- Intensive care patient that requires tracheal intubation for any indication
Exclusion criteria
- Decided not suitable for any reason by the intensivist.
- Under 18 years of age
If the checklist, for any reason, is not used for a patient after the implementation period, the data will still be included in the group of the second phase, since we believe the ICU staff will be considerably exposed to the checklist and hence, influenced by it.
Description of project This observational retrospective study will be conducted in the ICU, Karolinska University Hospital, Solna. The aim is to study whether introducing and implementing a pre-intubation checklist are associated with a lower incidence of intubation-related adverse events.
Adult ICU patients requiring intubation for any indication will be included, with inclusion and exclusion criteria as described above.
In a quality registry of ICU intubations, parameters such as pulse, blood pressure and SpO2 prior to, during and up to 5 minutes after intubation are manually registered from the monitor and put into the "ICU Respiration database". In addition, other intubation-related information is also registered, for instance: duration of intubation, airway assessment, intubation difficulty scale, intubation method and equipment, preoxygenation and intubation-related complications.
The study will consist of two phases. During the second phase, a checklist will be introduced and implemented based on the review of ICU airway guidelines and available literature. Physicians, residents and ICU nurses will receive information regarding the checklist prior to the intervention phase. If the checklist is not used for a patient during the second phase, the data will still be used in the cohort of the second group.
Data will be collected using the same intubation protocol as before the checklist introduction, containing patient demographics, the reason for ICU admission and intubation and vital parameters (saturation, blood pressure, pulse) before, during and after intubation. Blood gas analysis for arterial oxygen and carbon dioxide partial pressure will be analysed prior to intubation and in the immediate period after intubation (clinical practice). Furthermore, outcomes that will be registered are immediate complications such as desaturation, arterial hypotension, severe cardiac arrhythmia, cardiac arrest, death, oesophageal intubation, regurgitation, or a need for a surgical airway. Information regarding preoxygenation method, intubation circumstances and vasopressor use will be gathered, as well as 30-day mortality, length of hospital stay and ventilator days. Scores for physiological compromise ( and length of intensive care prior to intubation will be noted. Intubation-related data include the number of intubation attempts, Cormack-Lehane grade, time to end-tidal CO₂, the experience of the intubating physician, intubation difficulty scale, need for an alternative airway management and change of operator.
In both groups, the duration and method for preoxygenation and the drugs for anaesthetic induction are chosen as appropriate by the responsible intensivist.
Data will be collected from Clinisoft, the intensive care patient chart, regarding all intubations during the study period to find how many patients out of the total cohort that is not included during the study period.
The primary outcome is a comparison of intubation-related hypoxemic and hypotensive events between the two groups. Secondary events as severe arrhythmias, cardiac arrest, fatality and the number of intubation attempts will be analysed.
Statistics Data will be expressed as mean ± SD, median and range, 95% confidence intervals or number and percentage as appropriate. Comparison of two proportions will be performed using the chi-square test or Fischer exact test, where appropriate. Comparison of means will be performed using the student's t-test, while the comparison of medians will be analysed with the Mann-Whitney test. A p-value of <0.05 will be considered significant. Since this is a two-phase observational study of implementing a quality enhancing tool, it is, therefore, impossible to perform a correct power calculation. All the data, as mentioned above, will be compared between the two groups.
Clinical relevance Endotracheal intubation entails a significant risk of life-threatening complications in the intensive care setting. Therefore, optimising this procedure is of utmost importance. We aim to study whether the introducing and implementing a structured checklist for intubation will increase the safety of this standard yet perilous procedure. This could reduce the incidence of severe intubation-related complications and greatly benefit ICU patients.
Study design
- Observational model
- Cohort
- Time perspective
- Other
- Target follow-up
- 3 Months
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Standard care | – | Other: ChecklistIntubation procedure before introduction of a checklist |
| Checklist group | – | Other: ChecklistIntubation procedure after introduction of a checklist |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Intensive Care Patients that undergo tracheal intubation. All patients (before and after checklist) are registered with a protocol during intubation. This protocol is registered in a Respiratory Database.
Key inclusion criteria (2 listed)
- Patient in the ICU
- Need for tracheal intubation
Key exclusion criteria (2 listed)
- Pateint is under 18 years of age
- Patiend inclusion is decided not suitable for any reason by the intensivist
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ChecklistA checklist for the intubation procedure was organised into the categories physiological optimisation, equipment and drugs, team line-up, and contingency plan. This checklist was implemented in the clinic. | Other | Checklist group, Standard care |
Primary outcome
Level of desaturation
Time frame: From intubation up to 5 minutes after the procedure
- Peripheral oxygen saturation (SpO2) below 90% (or >5% drop if saturation is <90% after preoxygenation).
Level of lowering blood pressure
Time frame: From intubation up to 5 minutes after the procedure
A systolic arterial pressure (SAP) below 90 mmHg
11 secondary outcomes
30-day mortality
Time frame: 30 days
Ventilator days
Time frame: 30 days
Days in the intensive care unit
Time frame: 3 months
Number of intubation attempts
Time frame: 1 hour
First-pass success rate
Time frame: 1 hour
Lowest median oxygen saturation
Time frame: From induction of anaesthesia until up to 5 min after intubation?
Number of arrythmias
Time frame: Up to 5 min after intubation
Presence of cardiac arrest
Time frame: Up to 5 minutes after intubation
Change of intubation method
Time frame: 1 hour
Change of operator during intubation?
Time frame: During intubation
Intubation time
Time frame: 5 minutes
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 15 May 2026.
- Derived from this study: PubMed 40692385Nejatian A, Forsberg IM, Thoro U, Sjoblom A, Kahlin J. Impact of Checklist Implementation on Endotracheal Intubation-Related Complications in Critically Ill Adults-A Retrospective Before and After Study. Acta Anaesthesiol Scand. 2025 Aug;69(7):e70103. doi: 10.1111/aas.70103.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Critical Illness and Respiratory Failure, run by Karolinska University Hospital at 1 site in Sweden.
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 2 inclusion and 2 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: finished, as of the sponsor's last update on 15 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 Sweden. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Level of desaturation (time frame: From intubation up to 5 minutes after the procedure). The study lists 2 primary outcomes in all. 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 NCT06791317, which also lists 1 linked publication.
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 15 May 2026.