Clinical Trials Directory

Trials / Unknown

UnknownNCT04446715

Comparison of Meperidine and Sufentanil Added to 0.5% Hyperbaric Bupivacaine for Spinal Anesthesia in Cesarean Section

Comparison of Clinical Effects of Meperidine and Sufentanil Added to 0.5% Hyperbaric Bupivacaine for Spinal Anesthesia in Patients Undergoing Cesarean Section

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Makassed General Hospital · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Subarachnoid block is a widely used anesthetic technique for cesarean section. To improve the quality of analgesia and prolong its duration, the addition of intrathecal opioids to local anesthetics has been encouraged. In a double blind randomized controlled trial, 60 parturient women ASA 2-3 scheduled for elective cesarean delivery under spinal anesthesia will be randomly divided into 2 groups: Group 1 will receive sufentanil 5 μg and Group 2 will receive meperidine 12.5 mg. In every group, 0.5% heavy bupivacaine 10 will be added.

Detailed description

A questionnaire will be used to collect data. Patients' demographic and operative characteristics will be recorded. These include block level, heart rate, mean arterial pressure, nausea, vomiting, shivering and use of vasopressors. Post-operative data include pain, analgesic consumption, nausea and vomiting, as well as patients and surgeons satisfaction.

Conditions

Interventions

TypeNameDescription
DRUGsufentanilPatients will receive sufentanil in spinal anesthesia
DRUGmeperidinePatients will receive meperidine in spinal anesthesia
DRUGBupivacainePatients will receive 0.5% heavy bupivacaine in spinal anesthesia

Timeline

Start date
2020-10-01
Primary completion
2021-08-01
Completion
2021-08-01
First posted
2020-06-25
Last updated
2021-07-30

Locations

1 site across 1 country: Lebanon

Source: ClinicalTrials.gov record NCT04446715. Inclusion in this directory is not an endorsement.