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Osteopathy and Obstructive Sleep Apnea Syndrome II | Clinical Trials | Clareo Health

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COMPLETEDPhase 3NCT01822743

Osteopathy and Obstructive Sleep Apnea Syndrome II

The main objective is to evaluate an osteopathic compression of pterygopalatine node in healthy subjects and patients suffering from obstructive apnea syndrome (OSA).

Lead sponsor: Assistance Publique - Hôpitaux de Paris•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Assistance Publique - Hôpitaux de Paris

Osteopathic compression will be compared to a sham manoeuvre in a cross over design on apnea hypopnea index, pharyngeal collapsibility and symptoms in patients suffering from OSA, and on symptoms and pharyngeal collapsibility in healthy subjects.

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•Obstructive sleep apnea syndrome patient:
•Male or Female aged 18 years or more
•Obstructive sleep apnea syndrome with apnea/hypopnea index \> or = 15/hour
•Body mass Index \<40kg/m2
•Male or Female aged ≥18 and ≤ 40 years
•No obstructive sleep apnea syndrome
•Body mass Index \<30kg/m2
•No chronicle respiratory, neurological, cardiac or able to deteriorate sleep quality disease
•Low obstructive sleep apnea syndrome probability measured with Berlin Scale

Exclusion Criteria

•Pregnant or lactating women
•Participating to another trial
•Acute infectious disease of upper respiratory airway tract at inclusion
•Complete nasal obstruction
•Facial neuralgia at inclusion
•Patients not able to stop treatment for OSA within one week before each visit
•Allergy to latex
•Dental extraction within 15 days before inclusion
•Pharyngeal surgery in the past
•Incapable adult
•Patients treated with Selective Serotonin Reuptake Inhibitor
•Healthy Volunteers
•Pregnant or lactating women
•Participating to another trial
•Acute infectious disease of upper respiratory airway tract at inclusion
•Complete nasal obstruction
•Facial neuralgia at inclusion
•allergy to latex
•dental extraction within 15 days before inclusion
•pharyngeal surgery in the past
•incapable adult
•patients treated background treatment

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: January 25, 2022Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE3

Enrollment52

Start dateJan 2012

Last updatedJan 25, 2022

Condition

Obstructive Sleep Apnea Syndrome

Locations shown

Service des pathologies du sommeil, Pitié-Salpêtrière hospital

Paris

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 25, 2022Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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