To investigate the effect of dexmedetomidine and fentanyl on spinal analgesia
Phase 3
- Conditions
- Cesarean section.
- Registration Number
- IRCT20110313006044N2
- Lead Sponsor
- Bandare-abbas University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 110
Inclusion Criteria
Candidate for elective cesarean section and gestational age = 37 weeks
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method . Timepoint: . Method of measurement: .