The purpose of this study is to determine whether combined anesthesia will provide better pain control for the postoperative period following gynecological laparoscopy surgery.
Following signing an informed consent patients who are scheduled for gynecological laparoscopy surgery for benign disease will randomized to general vs. combined general and spinal anesthesia. During the postoperative period data regarding pain level as evaluated by visual analogue scale (VAS), number of doses of pain relief drugs, satisfaction and number of day in hospitalization will be collected from patient charts.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
40
Fentanyl 15 microgram Morphine 0.1-0.5 mg
Rambam Health Care Campus
Haifa, Israel
RECRUITINGRambam Health Care Campus
Haifa, Israel
NOT_YET_RECRUITINGPain level
Pain level will be evaluated every 4 hours from the time of surgery to discharge
Time frame: For the first 72 hours following surgery
Number of doses of analgesic drugs
Number of doses of analgesic medications will be collected from patients charts.
Time frame: For the first 72 hours following surgery
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