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Nasal Deformity, Acquired clinical trials

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NCT ID: NCT03726723 Not yet recruiting - Nasal Obstruction Clinical Trials

Effect of a Pre-Operative Local Anesthetic Facial Block on Post-Operative Rhinoplasty Pain

Start date: December 2018
Phase: Phase 4
Study type: Interventional

The specific aim of this study is to determine whether pre-operative treatment with a bupivacaine nerve block can influence post-operative pain and oxycodone usage among rhinoplasty patients. Specifically, we plan to directly compare the reported pain scale, nausea, and oxycodone usage among patients who received the bupivacaine block against those of patients in the saline control condition. These assessments will be documented on day 0 (day of operation) by a nurse in the Post-Anesthesia Care Unit, while the same data points will be collected over the phone by our clinical research coordinator on post-operative days 1, 2 , 3, and 8 following discharge.