Intravenous Versus Intraperitoneal Instillation of Ondansetron for Decreasing Incidence of Nausea and Vomiting After Laparoscopic Gynecological Surgeries.
Prevention
About this trial
This is an interventional treatment trial for Prevention
Eligibility Criteria
Inclusion Criteria:
- Written informed consent from the patient.
- Age: 21-45 years old.
- Both sex.
- Physical status: ASA 1& II.
- BMI = (25-35 kg/m2).
- Type of operation: elective laparoscopic gynecological surgeries.
Exclusion Criteria:
- Altered mental state.
- Patients with known history of allergy to the study drugs.
- Advanced hepatic, renal, cardiovascular, and respiratory diseases.
- Patients with chronic pain received NSAID or opioid during previous two weeks.
- Patients with history of PONV or motion sickness and patients received antiemetic therapy 24 h before the surgery.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Sham Comparator
Intraperitoneal instillation of ondansetron and bupivacaine (group A)
Intravenous ondansetron and intraperitoneal instillation of bupivacaine (group B)
Intraperitoneal instillation of bupivacaine (group C)
Patients will receive intraperitoneal instillation of (100 mg) 20 ml of bupivacaine 0.5 % and (4 mg) 2 ml ondansetron through abdominal ports by simple instillation technique before removal of trocars then clamping of abdominal drains for 1h to avoid drainage of LA.
Patient will receive intravenous (4 mg) 2 ml ondansetron and intraperitoneal instillation of (100 mg) 20 ml of bupivacaine 0.5 % through abdominal ports by simple instillation technique before removal of trocars then clamping of abdominal drains for 1h to avoid drainage of LA.
patient will receive intraperitoneal instillation of (100 mg) 20 ml of bupivacaine 0.5 % through abdominal ports by simple instillation technique before removal of trocars then clamping of abdominal drains for 1h to avoid drainage of LA.