Long Follow up on Patients With Obstructive Sleep Apnea That Undergo Diagnosis and Surgical Treatment

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02976207

Acronym

OSA

Enrollment

200

Registered

2016-11-29

Start date

2017-01-31

Completion date

Unknown

Last updated

2016-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

OSA

Brief summary

Long follow up on patients with obstructive sleep apnea that undergo diagnosis and surgical treatment

Detailed description

Drug induced sleep endoscopy (DISE) is increasingly performed procedure, offering dynamic upper airway evaluation during artificial sleep before surgical treatment for patients with obstructed .)OSA(sleep apnea * Aim: To evaluate the value of DISE for tailoring the proper treatment for patients with snoring and OSA DISE is a safe procedure, easily practicable, valid and reliable. We consider it a fundamental clinical procedure that is essential before choosing the surgical treatment. Our results so far suggest that a multilevel collapse is significantly associated with higher apnea hypopnea index values. We think that the weight did not play a significant role in RDI (Respiratory Disturbance Index) reduction. Our results till now show tailored surgery based on DISE may leverage sleep surgeries outcome significantly presenting 70% success rate based * on our experience We therefore want to evaluate the patients in a long follow up period

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 90 Years

Healthy volunteers

Inclusion criteria

* Fully diagnosed patients with OSA. * Patients who are candidates for a surgery as a treatment to their condition.

Exclusion criteria

* Pregnancy * Patients who are not OSA surgery candidates. * Patients with high surgical risk. * Patients with hematological or oncological background.

Design outcomes

Primary

Measure	Time frame
Measurement of daytime sleepiness- using Epworth sleepiness scale questionnaire	up to 3 years after surgery
Sleep quality assessment questionnaire	up to 3 years after surgery

Countries

Israel

Outcome results