Obstructive Apnea in Patients Submitted to Partial Laryngectomy

March 9, 2018 updated by: Hospital do Servidor Publico Estadual
The investigators intend to study the prevalence of obstructive apnea in patients submitted to partial laryngectomy by larynx cancer. Volunteers will be evaluated using polissonografy. We will try to correlate the residual glotic area with the number of apneas per hour.

Study Overview

Status

Unknown

Conditions

Detailed Description

We are trying to avaliate the residual glotic area using spirometry e laryngoscopy

Study Type

Observational

Enrollment (Anticipated)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • Brazil
      • São Paulo, Brazil, 040039901
        • Recruiting
        • Instituto de Assistência Médica ao Servidor Público Estadual
        • Contact:
        • Principal Investigator:
          • raquel teixeira, resident

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

PATIENTS OVER 18 YEARS, SUBMITED IN THE LAST 15 YEARS TO PARTIAL LARINGECTOMY IFNO TRACHEOSTOMY IS PRESENT

Description

Inclusion Criteria:

  • PARTIAL LARINGECTOMY, OVER 18 YEARS,

Exclusion Criteria:

  • TRACHEOSTOMY DEPRESSION USE OF DRUGS SEVERE DPOC CANCER RECURRENCE

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
level of apnea
patients will be separated depending on the iah(apnea hypopnea index) in mild, moderate and severe

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Hospital do Servidor Publico Estadual

Investigators

  • Principal Investigator: raquel teixeira, doctor, HSPE
  • Principal Investigator: Raquel Teixeira, doctor, pos graduatin student

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2010

Primary Completion (Anticipated)

July 1, 2011

Study Completion (Anticipated)

October 1, 2011

Study Registration Dates

First Submitted

July 6, 2010

First Submitted That Met QC Criteria

July 6, 2010

First Posted (Estimate)

July 7, 2010

Study Record Updates

Last Update Posted (Actual)

March 12, 2018

Last Update Submitted That Met QC Criteria

March 9, 2018

Last Verified

July 1, 2010

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • SAOS1

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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