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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00176683
Other study ID # 0120010351
Secondary ID
Status Terminated
Phase N/A
First received September 13, 2005
Last updated January 26, 2017
Start date July 2005
Est. completion date January 2009

Study information

Verified date January 2017
Source Rutgers, The State University of New Jersey
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess if capnography can be utilized to assist in the process of endotracheal intubation; specifically, in locating the glottic opening. Ultimately this would result in a new use of capnography to aid in securing normal and difficult airways. Currently capnography is only utilized for the confirmation of endotracheal tube placement.

If successful, this study will provide information, and allow for the development of instrumentation that will assist in difficult airway management; specifically, in locating the glottic opening when visualization may be impaired. Ultimately, this technique will be useful for routine and emergency airway management.


Description:

The purpose of this study is to assess if capnography can be utilized in the process of endotracheal intubation; specifically, in locating the glottic opening. Ultimately this would result in a new use of capnography to aid in securing normal and difficult airways. Currently capnography is only utilized for the confirmation of endotracheal tube placement.

If successful, this study will provide information, and allow for the development of instrumentation that will assist in difficult airway management; specifically, in locating the glottic opening when visualization may be impaired. Ultimately this technique will be useful for routine and emergency airway management.


Recruitment information / eligibility

Status Terminated
Enrollment 20
Est. completion date January 2009
Est. primary completion date September 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients for elective surgery, requiring general endotracheal anesthesia

Exclusion Criteria:

- Patients with a known or suspected difficult intubation

- Patients requiring specialized endotracheal tubes

- Patients with a history of tracheostomy

- Airway tumor or airway pathology

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Capnography
device which measures carbon dioxide at intubation

Locations

Country Name City State
United States New Jersey Medical School Newark New Jersey

Sponsors (1)

Lead Sponsor Collaborator
Rutgers, The State University of New Jersey

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary successful intubation at intubation
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