Clinical evaluation the effect of Xylapi ointment and lidocaine spray on the patient's satisfaction, stress, cooperation and pain level in spinal anesthesia for cesarean section and comparing it with the control group
Phase 3
Recruiting
- Conditions
- caesarean section.
- Registration Number
- IRCT20230128057251N1
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 258
Inclusion Criteria
Pregnant women referred to Bharlo Hospital with a gestational age of more than 37 weeks who are candidates for elective cesarean section
Exclusion Criteria
Gestational age below 37 weeks
Pregnant women who are candidates for emergency cesarean section
Pregnant women with chronic hypertension and diabetes
History of allergy to lidocaine
History of addiction and contraindications for spinal anesthesia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of mother's pain during spinal needle insertion. Timepoint: After caesarean section. Method of measurement: Visual Analog Scale.;The level of mother's satisfaction during transfer to the ward (end of recovery). Timepoint: After caesarean section. Method of measurement: Visual Analog Scale.;The level of mother's anxiety before the insertion of the spinal needle. Timepoint: After caesarean section. Method of measurement: Visual Analog Scale.;The level of cooperation of the mother according to the anesthesiologist. Timepoint: After caesarean section. Method of measurement: Anesthesiologist grading from 1 to 10.
- Secondary Outcome Measures
Name Time Method