Recruiting NCT07574905
Evaluation of Satisfaction and Experiences in Patients Undergoing Awake Intubation.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: awake intubation.
- Who it may be relevant to
- Registry conditions: Awake Endotracheal Intubation. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The aim of this observational study is to evaluate postoperative satisfaction and experiences in patients undergoing awake intubation.
Interventions
- Other awake intubation
To evaluate the experiences and satisfaction of patients who underwent awake intubation.
Primary outcome measures
- An assessment of patient satisfaction and experiences with the procedure in patients undergoing awake intubation using a questionnaire. [Time frame: 24 hours postoperatively]
Eligibility criteria
Inclusion criteria
- Be eligible for awake intubation
- Agree to participate in the study
- Be aged 18 or over
Exclusion criteria
- Having communication difficulties.
- Patients requiring emergency surgery.
- Refusing to take part in the study.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
Turkey (Türkiye) · 1 center
- Hacettepe University — Çankaya
Identifiers
NCT: NCT07574905 · SBA 24/272