Trials / Recruiting
RecruitingNCT07244757
Comparison of Two Dosing Regimens of Intravenous Ketorolac for Post-Cesarean Pain Control
Comparison of Two Dosing Regimens of Intravenous Ketorolac for Post-Cesarean Pain Control: A Randomized Controlled Trial
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 126 (estimated)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- 18 Years – 35 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
Spinal anesthesia will be achieved by injecting 10 mg hyperbaric bupivacaine 0.5% plus 25 mcg fentanyl Prophylactic vasopressor will be administered in all patients, Following delivery, all patients will receive a single dose of dexamethasone (8 mg) along with the first dose of intravenous ketorolac. Subsequent ketorolac doses will be administered every 8 hours. After closing the fascia, the subcutaneous layer will be infiltrated with 30 mL of 0.25% bupivacaine. Postoperatively, if the Numeric rating scale is \> 3, intravenous nalbuphine 0.1 mg/kg titrated to response, with maximum single dose of 20 mg and maximum daily dose of 160 mg.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ketorolac 30 mg | administered intravenously as 30 mg diluted in 10 mL of normal saline and injected over more than 15 seconds |
| DRUG | Ketorolac 15mg | administered intravenously as either 15 mg diluted in 10 mL of normal saline and injected over more than 15 seconds. |
Timeline
- Start date
- 2025-12-01
- Primary completion
- 2026-03-01
- Completion
- 2026-03-01
- First posted
- 2025-11-24
- Last updated
- 2026-01-13
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT07244757. Inclusion in this directory is not an endorsement.