Clinical trial comparing lidocaine 5% with fentanyl and Marcaine on the duration of spinal anesthesia in pregnant wome
Phase 2
- Conditions
- Condition 1: Spinal Anesthesia in pregnant patient. Condition 2: Spinal Anesthesia in pregnant patient.094-099
- Registration Number
- IRCT201707157745N9
- Lead Sponsor
- Vice chancellor for research, YUMS
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
Pregnant patients who come to the operating room for non-emergency c/s.
Exclusion criteria: patients with a history of diabetes, addiction, drugs are sedatives and psychoactive drugs.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The duration of analgesia after spinal anesthesia with lidocaine 5% with fentanyl and Marcaine in pregnant women undergoing cesarean section. Timepoint: 5 minutes after completion of caesarean section, Back pain at the site of action. Method of measurement: Touch the place.
- Secondary Outcome Measures
Name Time Method Satisfaction and a pleasant feeling by the mother. Timepoint: After the surgery and recovery time. Method of measurement: Ask the patient and see the clinical symptoms.