Anaesthesia
Conditions
Interventions
intrathecal morphine
Quadratus lumborum block
Sponsors
non
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: After approval of the hospital ethics committee, written informed consent was obtained from 90 ASA physical status II parturients; between the age of 19 and 40 years with a gestation of 37 weeks or more and normal singleton pregnancy, scheduled for elective C.S. via a Pfannenstiel incision under spinal anesthesia
Exclusion criteria
Exclusion criteria: The exclusion criteria were as follows: history of allergy to any relevant drug, body mass index >35 kg/m2, coagulopathy, chronic pain disorders, pregnancy-induced hypertension, gestation diabetes mellitus, and opioids abuse.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measure of this clinical study was the integrated analgesia assessment score | — |
Secondary
| Measure | Time frame |
|---|---|
| the secondary outcome measures were morphine consumption in the first 48 hours, NRS pain scores at 2h, 6h, 12h, 24h, 36h, and 48h , time to first ambulation, patient’s satisfaction, and morphine related side effects including nausea and vomiting, sedation, pruritis, and respiratory depression. | — |
Countries
Egypt
Contacts
Public ContactEman Salama
Lecturer of anesthesia and surgical ICU
Outcome results
None listed