Endoscopic sinus surgery (ESS) is a common otolaryngologic procedure that aims to remove the partitions that separate the sinus cavities, remove inflamed tissue, and optimize the sinuses for topical medication use. In this procedure, the surgeon will inject a combination of drugs, local anesthetics, and vasoconstrictors, to reduce bleeding and improve visualization. However, previous studies have shown similar results when injected with only saline. In this study, investigators want to determine if the injection of local anesthesic+vasoconstrictor compared to no injection at all makes any difference in improving the surgeon's visualization during an ESS.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
80
The combination contains 0.25% bupivacaine hydrochloride (2.5 mg/mL) and epinephrine bitartrate \[(1:200,000) 5 mcg/mL\] per vial.
Punctures without any medication injected onto the septum
St.Paul's Hospital Sinus Center
Vancouver, British Columbia, Canada
RECRUITINGBoezzart bleeding score
Change in mean surgical field quality as determined by the Boezzart bleeding score. Boezaart score of 0 indicates no bleeding, whereas the maximum score of 5 indicates severe bleeding (constant suctioning required).
Time frame: throughout study completion, one day study visit
Total blood loss
Change in total blood between injection and sham group measured in millilitres
Time frame: throughout study completion, one day study visit
Surgical time
Change in surgical time between injection and sham group measure in minutes
Time frame: throughout study completion, one day study visit
Mean arterial pressure (MAP)
Change in Mean arterial pressure (MAP) between injection and sham group measured in millimeters of mercury (mm Hg)
Time frame: throughout study completion, one day study visit
Postoperative bleeding
Change in postoperative bleeding between injection and sham group measured in mililiters
Time frame: throughout study completion, one day study visit
Postoperative pain
Change in postoperative pain between injection and sham group measured with a Visual Analog Scale (VAS) grading from 0 (no pain) to 5 (severe pain)
Time frame: throughout study completion, one day study visit
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