About this trial
This study aims to detect the effect of different O2 flow rates on end tidal carbon dioxide level in patients scheduled for minor gynaecological procedures under deep sedation using laryngeal mask airway.
* Primary outcome was measuring end tidal carbon dioxide ( EtCO2 ) non invasively by laryngeal mask all through the procedure. * Secondary outcomes included peripheral O2 saturation, hemodynamics, time to recovery, total propofol dose, patients' satisfaction, sedation score, and complications.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patient aged 18-45 years
ASA physical status l : ll
Minor elective gynaecological procedures lasting less than 30 minutes ( D&C biopsy, hysteroscopic polypectomy and diagnostic hysteroscopy )
Disqualifiers
Patient refusal to participate in this study.
ASA lll or more.
Lengthy procedures taking more than 30 minutes
Contraindication for the use of laryngeal mask airway as ( pharyngeal pathology, risk of aspiration and airway obstruction below larynx)
Trial population
females aged between18 - 45 years old scheduled for minor gynaecological procedures under deep sedation
Trial design
Cohort
Prospective
Treatments tested in this trial
capnography
Devicemeasurment of end-tidal carbon dioxide
Treatment groups
Trial outcomes
Primary outcomes
carbon dioxide monitoring
Primary outcome is measuring end tidal carbon dioxide ( EtCO2 ) non invasively by laryngeal mask all through the procedure.
Secondary outcomes
peripheral O2 saturation
peripheral O2 saturation
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: