Intrathecal Morphine for Cesarean Delivery

Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2021
This is a randomized double blinded non-inferiority study comparing the duration of pain relief when patients receive one of three doses of spinal morphine. Enrolled patients will be randomly assigned to receive either 50 mcg, 150 mcg, or 250 mcg. All patients will receive standardized postoperative care, including multimodal analgesia. The primary outcome will be the time until the patient requests additional opioid pain medications.
Epistemonikos ID: bdfb3c837a55a7fedf4e628b0edd5851ca22565c
First added on: May 09, 2024