- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT03024723
Nasal Continuous Positive Airway Pressure and Airway Patency in Obese Patient
Comparison of Upper Airway Patency Using Continuous Positive Airway Pressure Ventilation Via a Nasal Mask With a Face Mask During Induction of Anesthesia on Obese Patients
Panoramica dello studio
Descrizione dettagliata
Upper airway obstruction (UAO) is an unpredictable and frequently occurring complication during induction of general anesthesia. Since obese patients are more vulnerable to develop airway obstruction either during sleep1 or under anesthesia, and the segment of obese individuals in the entire population keep growing, difficult airway management under anesthesia becomes even more challenging than ever. The most serious event related to difficult airway management under anesthesia is "cannot intubate, cannot ventilate".
The mechanism of UAO during anesthesia has not been well understood. Obese patients are a high-risk group for perioperative airway catastrophe and prone to develop progressively narrower pharyngeal airways due to an increase of soft tissue volume surrounding the pharyngeal airway. The mechanism of UAO during anesthesia shares many similarities with the upper airway obstruction observed during obstructive sleep apnea (OSA). Nasal continuous positive airway pressure (nCPAP) via nasal mask (NM) can maintain the airway patent with near 100% success in patients with OSA. Obesity is a major risk factors for obstructive sleep apnea and obese patients have a higher prevalence of UAO during anesthesia. Therefore, the investigators hypotheses that nCPAP should eliminate airway obstruction in obese patients under anesthesia. The investigators propose to test this hypothesis and determine the efficacy of nCPAP on maintaining airway patency in obese patients who require general anesthesia.
Tipo di studio
Iscrizione (Effettivo)
Contatti e Sedi
Luoghi di studio
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Massachusetts
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Boston, Massachusetts, Stati Uniti, 02114
- Massachusetts General Hospital
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Metodo di campionamento
Popolazione di studio
Descrizione
Inclusion Criteria:
Body Mass Index:30 to 50 kg/ m2, Age: 18-65 years old ASA physical status classification: I-III Requiring general anesthesia for elective surgery
Exclusion Criteria:
- Patients with major cardiovascular disease, respiratory disease, cerebral vascular disease or American Society of Anesthesiologists physical status class IV or greater.
- Abnormal vital signs on the day of admission for surgery [heart rate (HR, >100 bpm or <40 bpm), blood pressure (BP, >180/100 mmHg or <90/60 mmHg), room air transcutaneous oxyhemoglobin saturation (SPO2) <96%] that are not correctable with his or her routine medication or commonly used pre-operative medication.
- Having claustrophobia and not able to tolerate the mask.
- Any person with an anticipated difficult airway or those with a history of difficult airway. This will include subjects who require or may require either a fiberoptic intubation or intubation while awake.
- Gastric-esophageal reflex disease that is refractory to treatment or a full stomach.
- The subject has been in bed for more than 24 hours.
- Neurological symptoms associated with neck extension, a neurological deficit from a previous stroke or spinal cord injury, a recent stroke or transient ischemic attack (TIA) within 2 weeks.
- Pregnant women and women less than one month post-partum. Ruling out pregnancy will be conducted by careful history and physical examination as performed routinely prior to surgery. If the history is believed to be unreliable, the patient will be excluded unless a pregnancy test is performed and the result of the test is negative.
Emergency cases and subjects who have not adhered to the ASA NPO (Nil Per Os) guidelines.
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Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
Intervento / Trattamento |
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FmCPAP
CPAP ventilation administered via face mask
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CPAP and ventilation administered via nasal mask
Altri nomi:
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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expired tidal volume
Lasso di tempo: 3 minutes
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This group of the subjects will start with nasal mask or face mask CPAP ventilation.
The anesthesia care team does whatever they routinely do, including adjusting the patient's position (as to reverse Trendelenburg position), pre-oxygenation, pre-medication, as usual with intravenous anesthetics and analgesics.
When the patient is apneic, CPAP ventilation will be initiated with pressure support mode at PIP 25 cmH2O, ventilation rate 10 BPM, PEEP 10 cmH2O and slope 1 second for 1 min.
If ventilation is effective in one of the first three breaths, the ventilation will continue for 1 min.
If effective ventilation cannot be produced in any of the first three breaths, the study will be terminated and routine care will be provided.
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3 minutes
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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expired tidal volume/Area under the Curve of the pressure trace
Lasso di tempo: 3 minutes
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The area under the airway pressure curve (AUC) defined as the area from the baseline pressure to the peak pressure during inspiration was calculated for evaluating pressure applied during inspiration.
The AUC is a reflection of the change in mean airway pressure.
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3 minutes
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Collaboratori e investigatori
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Completamento primario (Effettivo)
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Primo Inserito (Stima)
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Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 2013-P-000095/1
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Obeso
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Turku University HospitalUniversity of Turku; University of Helsinki; Hospital District of Helsinki and...ReclutamentoGravidanza | Controllo del peso | Postpartum | Usabilità | Donne incinte obese | Intervento digitaleFinlandia
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Cumhuriyet UniversityCompletatoFatica | Addestramento | Donne obeseTacchino
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Taipei City HospitalNational Yang Ming UniversitySconosciuto
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October 6 UniversityPharos University in AlexandriaCompletato
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Sibel ERDEMHacettepe UniversityCompletatoPerdita di peso | Donne obeseTacchino
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Clinical Nutrition Research Center, Illinois Institute...CompletatoDonne in premenopausa | Donne in sovrappeso e obeseStati Uniti
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Nicole StoffelAmerican University of Beirut Medical CenterReclutamentoDonne in sovrappeso e obeseLibano
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University of GlasgowReclutamento
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University Hospital, Clermont-FerrandCompletato
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Sabrin Mohamed Taha AbdelwahabCompletatoDonne obese con PCOSEgitto
Prove cliniche su nasal mask CPAP
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Vyaire MedicalM.D. Anderson Cancer CenterCompletatoIpossiemiaStati Uniti
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Fisher and Paykel HealthcareCompletatoApnea ostruttiva del sonnoStati Uniti
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Laboratoires Quinton International S.L.Non ancora reclutamentoRinite allergica | Congestione nasale | Raffreddore | Rinosinusite | Sintomo influenzaleSpagna
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Fundació Institut de Recerca de l'Hospital de la...CompletatoProgrammi per persone saneSpagna
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Weill Medical College of Cornell UniversityCompletatoApnea ostruttiva del sonno (OSA)Stati Uniti
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Fisher and Paykel HealthcareTerminatoObesità Sindrome da ipoventilazioneNuova Zelanda
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Pathway Medtech, LLC.Haku TechnologyReclutamentoApnea notturna | Qualità del sonno | Disturbi respiratori del sonno (SDB)Belgio
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Pathway Medtech, LLC.Non ancora reclutamentoApnea notturna | Disturbi respiratori del sonno (SDB)Stati Uniti
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Cairo UniversityNon ancora reclutamento
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Siperstein DermatologyCompletato