IRCT201707157745N9
Completed
Phase 2
Comparative study of the duration of analgesia following spinal anesthesia with lidocaine 5% with fentanyl and marcain in pregnant women under cesarean section
Vice chancellor for research, YUMS0 sites200 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Condition 1: Spinal Anesthesia in pregnant patient. Condition 2: Spinal Anesthesia in pregnant patient.
- Sponsor
- Vice chancellor for research, YUMS
- Enrollment
- 200
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Not specified
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