The Effect of Oxygen Flow Rate on End-tidal CO2 During Deep Sedation

ConditionCapnography
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorMinia University

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • capnography

    Device

    measurment of end-tidal carbon dioxide

Treatment groups

120 Participants
are divided into 3 treatment groups
Group A: Group A1 intervention
Group B: Group B1 intervention
Group C: Group C1 intervention

Trial outcomes

Primary outcomes

1

carbon dioxide monitoring

Primary outcome is measuring end tidal carbon dioxide ( EtCO2 ) non invasively by laryngeal mask all through the procedure.

Time frame
baseline and every 5 minutes all through the procedure

Secondary outcomes

1

peripheral O2 saturation

peripheral O2 saturation

Time frame
baseline and every 5 minutes all through the procedure

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: