Clinical Trials in Egypt / NCT07706348
Recruiting
Phase 1/2
Intraperitoneal Irrigation of Ondansteron in Combination With Lidocaine in Acute Postoperative Pain
NCT07706348 · tracked via the Priya Life Science Egypt tracker
Condition(s) studied
Acue Postoperative Pain
Investigational drug(s) / intervention(s)
ondansteron
ondansteron: intraperitonel irrigation
Study summary
This study, therefore, aimed to investigate the effect of intraperitoneal administration of ondansetron in combination to lidocaine for postoperative pain management in patients undergoing lower abdominal cancer surgery.
Eligibility
Inclusion Criteria:
* ASA I-II patients
* scheduled for major lower abdominal cancer surgeries.
Exclusion Criteria:
* patients with known allergy to the study drugs,
* significant cardiac, respiratory, renal or hepatic disease,
* body mass index (BMI) ≥30 kg/m2;
* allergy to study drugs
* history of opioid use for pain management the time of enrolment or drug addiction,
* who had used benzodiazepine chronically,
* stroke or psychiatric disease that could affect the perception of pain.
Primary outcome measure(s)
- total morphine consumption — in the first 24 hours postoperative
total amount of morphine consumption in mg in the first 24 hours for analgesia
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Assiut University - South Egypt Cancer Instiute | Asyut | Egypt | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07706348 on ClinicalTrials.gov ↗ ← All trials in Egypt