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A comparison of Propofol with ketofol (a Ketamine-Propofol combination) for sedation during hysteroscopy in patient in IVF operation room

Not Applicable
Conditions
Parenteral anaesthetics.
Parenteral anaesthetics
Registration Number
IRCT201105176510N1
Lead Sponsor
Ahwaz Jondi Shapur University of medical sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
40
Inclusion Criteria

age under 40y, ASA class 1&2, no cardiovascular risk factor, no history of reaction to egg or soy bean & Ketamine or propofol, no psychiatric history, no history of airway difficulty. Exclusion criteria: airway difficulty like difficult ventilation, change of hysteroscopy to open surgery or complicated hysteroscopy.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Depth of anesthesia. Timepoint: 5 minute after induction of anesthesia. Method of measurement: with Bispecteral Index Score device.
Secondary Outcome Measures
NameTimeMethod
Incidence of apnea. Timepoint: in time of anesthesia. Method of measurement: observation of anesthesiologist.;Incidence of nausea & vomiting. Timepoint: in time of anesthesia & recovery. Method of measurement: observation of anesthesiologist.;Systolic blood pressure. Timepoint: before & 5 minute after induction of anesthesia. Method of measurement: automatic blood pressure device.;Pulse rate. Timepoint: before & 5 minute after induction of anesthesia. Method of measurement: ECG monitoring device.;Psychiatric side effect. Timepoint: recovery period. Method of measurement: observation of anesthesiologist.
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