Awake Endotracheal IntubationNCT07574905
Evaluation of Satisfaction and Experiences in Patients Undergoing Awake Intubation.
An observational study of Awake Endotracheal Intubation, run by Hacettepe University at 1 site in Turkey (Türkiye).
Trial summary
The aim of this observational study is to evaluate postoperative satisfaction and experiences in patients undergoing awake intubation. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Awake Endotracheal Intubation
- What is being tested?
- awake intubation
- How many people
- 116 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 14 Apr 2026to 14 Sep 2026
- 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: adult patients
Who may be able to join
- Be eligible for awake intubation
- Agree to participate in the study
- Be aged 18 or over
Who cannot join
- Having communication difficulties.
- Patients requiring emergency surgery.
- Refusing to take part in the study.
Trial locations and contacts
1 site in 1 country.
About this study
The aim of this observational study is to evaluate postoperative satisfaction and experiences in patients undergoing awake intubation.
- Conditions
- Awake Endotracheal Intubation
- Being tested
- awake intubation
- Keywords
- Awake intubation, Difficult airway, Satisfaction, Experience
- Medical subject headings
- Personal Satisfaction
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
awake intubationOther
To evaluate the experiences and satisfaction of patients who underwent awake intubation.
What is being measured
The primary outcome is the main question the study is designed to answer.
An assessment of patient satisfaction and experiences with the procedure in patients undergoing awake intubation using a questionnaire.
Participants rate the questions on a scale from 1 to 5. A score of 1 is interpreted as 'very poor', and a score of 5 as 'very good'.
Measured: 24 hours postoperatively
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 May 2026
- Study start14 Apr 2026
- Primary completion30 Jun 2026
- Study completion14 Sep 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Awake Endotracheal IntubationStudies of the same condition, open and under way.
- More trials run by Hacettepe UniversityThe 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
- Case only
- Time perspective
- Prospective
- Enrolment
- 116 participants (actual)
Sponsor and investigators
- Lead sponsor
- Hacettepe University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ozge Ozen, Hacettepe University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07574905
- Sponsor's protocol ID
- SBA 24/272
- Status last verified
- May 2026
- First submitted
- 28 Apr 2026
- Last updated
- 18 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 18 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Satisfaction and Experiences in Patients Undergoing Awake Intubation.
- ClinicalTrials.gov ID
- NCT07574905
- Acronym / sponsor ID
- SBA 24/272
- Conditions
- Awake Endotracheal Intubation
- Keywords
- Awake intubation, Difficult airway, Satisfaction, Experience
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 116 participants (actual)
- Lead sponsor
- Hacettepe UniversityUniversity, hospital or other
- Study start
- 14 Apr 2026 (actual)
- Primary completion
- 30 Jun 2026 (actual)
- Study completion
- 14 Sep 2026 (actual)
- First posted
- 8 May 2026 (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.
The aim of this observational study is to evaluate postoperative satisfaction and experiences in patients undergoing awake intubation.
Study design
- Observational model
- Case only
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- adult patients
Key inclusion criteria (3 listed)
- Be eligible for awake intubation
- Agree to participate in the study
- Be aged 18 or over
Key exclusion criteria (3 listed)
- Having communication difficulties.
- Patients requiring emergency surgery.
- Refusing to take part in the study.
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 |
|---|---|---|
| awake intubationTo evaluate the experiences and satisfaction of patients who underwent awake intubation. | Other | – |
Primary outcome
An assessment of patient satisfaction and experiences with the procedure in patients undergoing awake intubation using a questionnaire.
Time frame: 24 hours postoperatively
Participants rate the questions on a scale from 1 to 5. A score of 1 is interpreted as 'very poor', and a score of 5 as 'very good'.
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 18 Sep 2026.
- Individual participant dataSharing planned: Undecided
Related trials for Awake Endotracheal Intubation
Recruiting
Comparison of Awake Tracheal Intubation Methods
Airway Management Assessment, Awake Endotracheal Intubation
Not yet recruitingObservational study
Emergence Delirium、fBFI-ENO Score (Extraversion + Neuroticism - Openness) Based on the Fast Big Five Personality Scale-10、An Adult Patient With ASAI-III Who is Scheduled for Elective Non-cardiac Surgery and is to Undergo General Anesthesia With Tracheal Intubation
Emergence Delirium, Anesthesia
Recruiting
Thyroid Cartilage Plane VS Superior Laryngeal Nerve Space Block in Awake Tracheal Intubation
Superior Laryngeal Nerve Block
Recruiting
High-flow Nasal Cannula Versus Conventional Oxygen During Awake Tracheal Intubation With Difficult Airways
Awake Tracheal Intubation, Difficult Airway
RecruitingObservational study
Patient Experience of Transoral Versus Transnasal Awake Tracheal Intubation
Airway Management, Fiberoptic Guided Intubation
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 Awake Endotracheal Intubation, run by Hacettepe University at 1 site in Turkey (Türkiye).
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 3 inclusion and 3 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 18 Sep 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 Turkey (Türkiye). 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?
An assessment of patient satisfaction and experiences with the procedure in patients undergoing awake intubation using a questionnaire. (time frame: 24 hours postoperatively). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 18 Sep 2026.