NCT04158323

Brief Summary

A prospective Observationalstudie to analyze the current significance of the awake flexible endoscopy in German hospitals.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2019

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

November 6, 2019

Completed
2 days until next milestone

First Posted

Study publicly available on registry

November 8, 2019

Completed
15 days until next milestone

Study Start

First participant enrolled

November 23, 2019

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 23, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 23, 2019

Completed
Last Updated

December 24, 2019

Status Verified

December 1, 2019

Enrollment Period

1 month

First QC Date

November 6, 2019

Last Update Submit

December 23, 2019

Conditions

Keywords

flexible endoscopyawake intubation

Outcome Measures

Primary Outcomes (1)

  • What is the current practice for Airway Management in patients with a anticipated difficult airway?

    Evaluation of the current practice to secure the airway in patients with a anticipated difficult airway

    through study completion, an average of 10 minutes

Secondary Outcomes (1)

  • What is the most preferred technique for awake flexible endoscopy?

    through study completion, an average of 10 minutes

Interventions

survey of anesthesists and intensive care physician of the perfomans with the flexible endoscope in patients with a anticipated difficult airway

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

anesthesists and intensive care physicians

You may qualify if:

  • experience in anesthesia or intensive care

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Anesthesiology,Prof. C. Werner, Universitätsmedizin of the JG University

Mainz, Rhineland-Palatinate, D55131, Germany

Location

MeSH Terms

Interventions

Airway Management

Intervention Hierarchy (Ancestors)

Therapeutics

Study Officials

  • Marc Kriege, MD

    University Medical Center Mainz

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

November 6, 2019

First Posted

November 8, 2019

Study Start

November 23, 2019

Primary Completion

December 23, 2019

Study Completion

December 23, 2019

Last Updated

December 24, 2019

Record last verified: 2019-12

Locations