Obstructive Apnea in Patients Submitted to Partial Laryngectomy

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2010 by Hospital do Servidor Publico Estadual.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Hospital do Servidor Publico Estadual
ClinicalTrials.gov Identifier:
NCT01157286
First received: July 6, 2010
Last updated: NA
Last verified: July 2010
History: No changes posted
  Purpose

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.


Condition Intervention
Obstructive Sleep Apnea
Device: CPAP

Study Type: Observational
Study Design: Observational Model: Ecologic or Community
Time Perspective: Retrospective
Official Title: Obstructive Apnea in Patients Submitted to Partial Laryngectomy

Resource links provided by NLM:


Further study details as provided by Hospital do Servidor Publico Estadual:

Estimated Enrollment: 20
Study Start Date: June 2010
Estimated Study Completion Date: October 2011
Estimated Primary Completion Date: July 2011 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
level of apnea
patients will be separated depending on the iah(apnea hypopnea index) in mild, moderate and severe
Device: CPAP
PATIENTS DIADNOSSED WITH MILD TO SEVERE APNEA WILL BE TREATED WITH CPAP

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

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

Criteria

Inclusion Criteria:

  • PARTIAL LARINGECTOMY, OVER 18 YEARS,

Exclusion Criteria:

  • TRACHEOSTOMY DEPRESSION USE OF DRUGS SEVERE DPOC CANCER RECURRENCE
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01157286

Contacts
Contact: RAQUEL C TEIXEIRA, RESIDENT 55 61 82222073 raquelch@bol.com.br
Contact: MICHEL B CAHALI, STAF 55 11 99519941 mcahali@gmail.com

Locations
Brazil
Instituto de Assistência Médica ao Servidor Público Estadual Recruiting
São Paulo, Brazil, 040039901
Contact: teixeira    55 61 82222073    raquelch@bol.com.br   
Principal Investigator: raquel teixeira, resident         
Sponsors and Collaborators
Hospital do Servidor Publico Estadual
  More Information

No publications provided

Responsible Party: Raquel Chartuni Pereira Teixeira, resident
ClinicalTrials.gov Identifier: NCT01157286     History of Changes
Other Study ID Numbers: SAOS1
Study First Received: July 6, 2010
Last Updated: July 6, 2010
Health Authority: Brazil: Ministry of Health

Keywords provided by Hospital do Servidor Publico Estadual:
OBSTRUCTIVE SLEEP APNEA LARINGECTOMY CPAP

Additional relevant MeSH terms:
Apnea
Sleep Apnea Syndromes
Sleep Apnea, Obstructive
Dyssomnias
Nervous System Diseases
Respiration Disorders
Respiratory Tract Diseases
Signs and Symptoms
Signs and Symptoms, Respiratory
Sleep Disorders
Sleep Disorders, Intrinsic

ClinicalTrials.gov processed this record on October 23, 2014