Post-laparoscopic pain, number of post-laparoscopic opioid consumption, post-laparoscopic nausea and vomiting..
Conditions
Interventions
Intervention 1: First intervention group: ?30 mg intravenous ketorolac (15 mg/ml, 2 ml) 30 min before the surgery. Intervention 2: Second intervention group: ?8 mg intravenous dexamethasone (4 mg/ml,
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age of 18-65 years Body mass index <30 kg/m2 American Society of Anesthesiologists grade I or II
Exclusion criteria
Exclusion criteria: Allergy to analgesics Anticoagulant consumption during the last four weeks before the surgery Daily intake of opioids or anti-anxiety medications Fever Bacterial infection within the last two weeks before the surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-laparoscopic pain. Timepoint: 1, 6, 12, and 24 hours after the laparoscopy. Method of measurement: Visual analog scale.;Opioid consumption. Timepoint: Within 24 hours after laparoscopy. Method of measurement: Recorded number in the patients' medical profile. | — |
Secondary
| Measure | Time frame |
|---|---|
| Post-laparoscopic nausea and vomiting. Timepoint: Within 24 hours after the surgery. Method of measurement: Patient's profile. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Asgari
Tehran University of Medical Sciences
Outcome results
None listed