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The effect of dexamethasone and endonestrone premedication on the incidence of nausea and vomiting after cesarean sectio

Phase 3
Recruiting
Conditions
nausea and vomiting.
Registration Number
IRCT20180210038681N1
Lead Sponsor
Khoram-Abad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
120
Inclusion Criteria

All patients who have attended for elective cesarean section
In the ASA class one and two
being in fertility age
Patients with normal, mild or moderate stress, anxiety and depression level
Patients who will undergo spinal anesthesia with bupivacaine 0.5%

Exclusion Criteria

Patients suffering from pregnancy toxicity ( eclampsia- preclampsia) or history of motion sickness, history of meniere disease, and migraine
BMI greater than 40
history of PONV( post opreative neusea and vomiting )
severe or very severe level Stress , anxiety and depression
Cigarette smoking and opoid drug consumption
Patients that donot to cooperate
Patients who undergo spinal anesthesia with lidocaine 5%
Patients who receive atropine during opreation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea. Timepoint: In PACU (at 0 oclock) and 2 oclock and after 6 oclock, the incidence of nausea and vomiting in the patient. Method of measurement: VAS ( Visual analog scale ).;Vomiting. Timepoint: At PACU (at the begining) and 2 hours and 6 hours later. Method of measurement: Interview with patient.;Stress, depression and anxiety. Timepoint: In the recovery before surgery. Method of measurement: Depression‚ Anxiety‚ Stress Scale (DASS).
Secondary Outcome Measures
NameTimeMethod
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