Comparison of Different Video Laryngoscopes in a Manikin With Immobilized Cervical Spine

NCT ID: NCT01210092

Last Updated: 2011-09-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-08-31

Study Completion Date

2011-01-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To determine whether different video laryngoscopes facilitate intubation in an manikin with immobilized cervical spine compared with standard laryngoscopy.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Tracheal Intubation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Macintosh #3 Laryngoscope

No interventions assigned to this group

Glidescope

No interventions assigned to this group

Ambu Pentax AWS

No interventions assigned to this group

McGrath

No interventions assigned to this group

Airtraq

No interventions assigned to this group

Storz C-MAC

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* anaesthesiologist
* experienced in tracheal intubation

Exclusion Criteria

* missing experience in tracheal intubation
* missing informed consent
Minimum Eligible Age

25 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Cologne

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

J. Hinkelbein

PD Dr. med.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Wolfgang A Wetsch, MD

Role: PRINCIPAL_INVESTIGATOR

Department of Anaesthesiology, University of Cologne

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Department of Anaesthesiology and Postoperative Critical Care

Cologne, , Germany

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Germany

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

10-182-2

Identifier Type: -

Identifier Source: org_study_id