Status:
COMPLETED
Comparison of Three Different Doses of Intrathecal Morphine for Analgesia After Cesarean Section
Lead Sponsor:
Ondokuz Mayıs University
Conditions:
Cesarean Section
Spinal Anesthesia
Eligibility:
FEMALE
18-40 years
Phase:
NA
Brief Summary
In our study, It was aimed to determine the dose of morphine that provides the most effective analgesia with the least incidence of side effects in the postoperative period.
Detailed Description
Spinal anesthesia is a widely used method in cesarean section operations. It has become a popular practice to add opioids to local anesthetic agents to improve the quality and prolong the duration of ...
Eligibility Criteria
Inclusion
- Patient undergoing cesarean section
- Between the ages of 18-40,
- ASA II,
- Pregnant women with gestational week \> 36
Exclusion
- Not accepting regional anesthesia,
- İnfection at the injection site,
- Coagulopathy, bleeding diathesis,
- Severe hypovolemia,
- İncrease in intracranial pressure,
- Pregnant women with problems such as severe aortic stenosis, severe mitral stenosis for which spinal anesthesia is contraindicated,
- Patients with a history of allergy to any drug included in the study protocol
Key Trial Info
Start Date :
October 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2020
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT05317572
Start Date
October 1 2017
End Date
September 1 2020
Last Update
April 15 2022
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Ondokuz Mayıs University Faculty of Medicine
Samsun, Turkey (Türkiye)