NCT07574905

Completed

Evaluation of Satisfaction and Experiences in Patients Under...

Hacettepe University Source

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Other study identifiers

Sponsor study identifier

SBA 24/272

Study Type

observational

Actual enrollment (reported)

116

Locations

1 country

Sites

1

Timeline

Study Start

April 14, 2026

Actual (reported)

Primary Completion

June 30, 2026

Actual (reported)

Study Completion

September 14, 2026

Actual (reported)

Brief Summary

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

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 116 participants
Study completion date: September 14, 2026
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

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Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
April 14, 2026
Actual (reported)
First Submitted
April 28, 2026
Actual (reported)
First Posted
May 8, 2026
Actual (reported)
Primary Completion
June 30, 2026
Actual (reported)
Study Completion
September 14, 2026
Actual (reported)

Last Updated: September 18, 2026
Status Verified: May 2026
Last Update Submitted: September 15, 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.

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

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

Sponsors & Collaborators

Hacettepe University
Otherlead

Study Sites (1)

Hacettepe University

Çankaya, Ankara, Turkey (Türkiye)

MeSH Terms

Conditions

Personal Satisfaction

Condition Hierarchy (Ancestors)

Behavior

Enrollment

116 participants (actual enrollment reported by the registry).

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

Actual (reported)

NCT01848548

Superior Laryngeal Nerve Block For Awake Endotracheal Intubation Study

Terminated

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.

Primary Completion

June 30, 2026

Actual (reported)

Study Completion

September 14, 2026

Actual (reported)

Last Updated

September 18, 2026

Record last verified: 2026-05

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT07574905
Data provider: ClinicalTrials.gov
Source updated: 2026-09-18
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:29:22 UTC

Documents

Study Protocol, Statistical Analysis Plan, and Informed Consent Form
ProtocolSAPICF2024-02-20

Locations

TR(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Documents

Locations