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NCT00883376 Clinical Trial

Classification of Stanford for Snore as Factor of Aggravation of the Apnea Hypopnea Index (AIH) in Patients With Obstructive Sleep Apnea Syndrome (OSAS)

Obstructive Sleep Apnea Syndrome Clinical Trial

— StanforAIH  

Official title:
Classification of Stanford for Snore as Factor of Aggravation of the AIH in Patients With OSAS.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00883376
Other study ID # CEP ISCML 114/08
Secondary ID StanforAIH
Status Completed
Phase N/A
First received April 16, 2009
Last updated April 16, 2009
Start date January 2007
Est. completion date December 2008

Study information
Verified date April 2009
Source Irmandade da Santa Casa de Misericoridia de Limeira
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Introduction: Obstructive sleep apnea syndrome (OSAS) became an important and prevalent illness in recent years. The population occidental becomes fat each time, and this symptom is associated the biggest risk for the OSAS. Snore presence is extremely associated with OSAS. Snoring is present in about 90 - 95% of the patients with OSAS.

Objectives: Evaluate the influence in the Stanford classification as predictor factor of gravity of the OSAS.

Materials and Methods: They evaluated and classified 107 patients, Classification of Mallampati, Friedman, Classification of Stanford and how much the gravity of the OSAS for the AIH.

Recruitment information / eligibility
Status Completed
Enrollment 159
Est. completion date December 2008
Est. primary completion date February 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- Not exhibiting any exclusion criteria

- Age > 21 years

Exclusion Criteria:

- Nasal tumor

- BMI >40

- Nasal polipose

- No acceptance of study

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Brazil Hospital Dia Limeira S

Sponsors (1)
Lead Sponsor Collaborator
Irmandade da Santa Casa de Misericoridia de Limeira

Country where clinical trial is conducted

Brazil, 

Outcome
Type Measure Description Time frame Safety issue
Primary Stanford Classification for snoring One year
Secondary Apnea-Hyponea Index one year
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