Comparison of Two Dosing Regimens of Intravenous Ketorolac for Post-Cesarean Pain Control

Sex: Female

Ages: 18 Years – 35 Years

Healthy volunteers: No

Phase: NA

Enrollment: 125

Sponsor: Cairo University

Summary

we aim to compare the analgesic efficacy of two intravenous ketorolac dosing regimens as part of a multimodal analgesic protocol that includes local wound infiltration for postoperative pain management after elective cesarean delivery.

Eligibility Criteria

Inclusion Criteria: * full-term, singleton, pregnant women, * aged 18-35 years, * scheduled for elective cesarean delivery under spinal anesthesia Exclusion Criteria: * American Society of Anesthesiologists (ASA) physical class III or more * multiple gestation. Patients with a history of allergy to any of the study drugs, * renal impairment, * gastrointestinal bleeding or ulceration * inflammatory bowel disease, * chronic pain or regular opioid use. * Inability to comprehend the numeric pain scale (NRS) or the ObsQoR-11 score * requirement for conversion to general anesthesia after spinal anesthesia

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07244757). StuddyBuddy aggregates publicly available trial information.