Cesarean section.
Conditions
Interventions
Intervention 1: Intervention group 1: 10mg bupivacaine 0.5% + 5mg dexmedetomedine(PrecedexTM 200mcg/2ml Hospira, Inc,lake Forest, IL60045USA). Intervention 2: Intervention group 2: 10mg bupivacaine 0.
Sponsors
Bandare-abbas University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
16 Years to 41 Years
Inclusion criteria
Inclusion criteria: Candidate for elective cesarean section and gestational age = 37 weeks
Exclusion criteria
Exclusion criteria: Emergency patients Patients with a ban on regional block Patients with heart valve disease Patients with a history of allergy to the drugs used Addictive or alcoholic patients Patients with placenta parvia Patients who require medication during surgery because of incomplete blockage
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain rate and duration of analgesia. Timepoint: Measurement of pain and duration of analgesia in recovery and during 6-3 hours after surgery. Method of measurement: Patients' severity of pain is based on the Visual Analogues Scale, with the left side indicating no pain and the right side showing the number "10" indicating the most severe pain. Score style 1-3 indicates mild pain, 4-7 moderate pain, severe pain 8-10), duration of analgesia from time to block until patient requests for analgesics. | — |
Secondary
| Measure | Time frame |
|---|---|
| . Timepoint: . Method of measurement: . | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHashem Jarineshin
Bandare-abbas University of Medical Sciences
Outcome results
None listed