NCT07574905

Brief Summary

The aim of this observational study is to evaluate postoperative satisfaction and experiences in patients undergoing awake intubation.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
1mo left

Started Apr 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress52%
Apr 2026Jun 2026

Study Start

First participant enrolled

April 14, 2026

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

April 28, 2026

Completed
10 days until next milestone

First Posted

Study publicly available on registry

May 8, 2026

Completed
24 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Last Updated

May 8, 2026

Status Verified

May 1, 2026

Enrollment Period

2 months

First QC Date

April 28, 2026

Last Update Submit

May 5, 2026

Conditions

Awake Endotracheal Intubation

Keywords

Awake intubationDifficult airwaySatisfactionExperience

Outcome Measures

Primary Outcomes (1)

  • 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'.

    24 hours postoperatively

Interventions

awake intubationOTHER

To evaluate the experiences and satisfaction of patients who underwent awake intubation.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

adult patients

You may qualify if:

  • Be eligible for awake intubation
  • Agree to participate in the study
  • Be aged 18 or over

You may not qualify if:

  • Having communication difficulties.
  • Patients requiring emergency surgery.
  • Refusing to take part in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hacettepe University

Çankaya, Ankara, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Personal Satisfaction

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Ozge Ozen

CONTACT

+905396674959drozgeozen09@gmail.com

Aysun Ankay Yılbas

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Doctor

Study Record Dates

First Submitted

April 28, 2026

First Posted

May 8, 2026

Study Start

April 14, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

May 8, 2026

Record last verified: 2026-05

Locations

TU(1)