Anxiolytic effect of N2O
Phase 2
- Conditions
- Childbirth Anxiety under spinal anesthesia.Mental and behavioural disorders associated with the puerperium, not elsewhere classified
- Registration Number
- IRCT2012091510841N1
- Lead Sponsor
- Hamadan University Of Medical Science, Vice chancellor for research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 56
Inclusion Criteria
primigravid patients; 18-45 years old; educated; scheduled for cesarean section under spinal anesthesia. Exclusion criteria: Pre-eclampsia & Eclampsia; Vavular Heart Disease; Respiratory Disease; Previous Nausea &Vomiting Ear Disease or Surgery; Increased ICP; Anemia; Shock; Patient refusal.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anxiety Level. Timepoint: Befor spinal anesthesia and During spinal anesthesia, Skin Incision, Uterine Incision, Birth Time, Recovery Time. Method of measurement: Anxiety VAS.
- Secondary Outcome Measures
Name Time Method Heart rate. Timepoint: every 5 minutes up to 15 minutes and every 15 minutes up to the end of the operation. Method of measurement: Puls oximetry.;Hallucination. Timepoint: During Surgery & Recovery Time. Method of measurement: Observation.;Nausea & Vomiting. Timepoint: During operation & Recovery Time. Method of measurement: Observation.;Systoilic & Diastolic Blood Pressure. Timepoint: every 5 minutes up to 15 minutes and every 15 minutes up to the end of the operation. Method of measurement: Non Invasive Blood Pressure Monitoring.