Classification of Stanford for Snore as Factor of Aggravation of the Apnea Hypopnea Index (AIH) in Patients With Obstructive Sleep Apnea Syndrome (OSAS)
NCT ID: NCT00883376
Last Updated: 2009-04-17
Study Results
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.
COMPLETED
159 participants
OBSERVATIONAL
2007-01-31
2008-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Correlation Between Friedman Classification and the Apnea Hypopnea Index (AIH) in a Population With Obstructive Sleep Apnea Syndrome (OSAS)
NCT00883025
Polysomnography and Heart Rate Indexes in Obstructive Sleep Apnea
NCT02044900
Upper Airway Obstruction in Non-obese Patients With Snoring and Obstructive Sleep Apnea
NCT04324671
Assessment of Obstructive Sleep Apnea Syndrome in Non-Obese Patients
NCT05814796
Voice Acoustic Properties in People With Obstructive Sleep Apnea Syndrome (OSAS)
NCT03568240
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
ECOLOGIC_OR_COMMUNITY
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
OSAS patients
No interventions assigned to this group
2
no OSAS patients
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.
Exclusion Criteria
* Nasal tumor
* BMI \>40
* Nasal polipose
* No acceptance of study
21 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Irmandade da Santa Casa de Misericoridia de Limeira
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Irmandade da Santa Casa de Misericoridia de Limeira
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hospital Dia
Limeira, S, Brazil
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
StanforAIH
Identifier Type: -
Identifier Source: secondary_id
CEP ISCML 114/08
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.