Overview
Ropivacaine and Bupivacaine in Sphenopalatine Ganglion Block in Sinus Surgery
Status:
Completed
Completed
Trial end date:
2014-12-01
2014-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Postoperative analgesia after FESS can be achieved through opioids, NSAIDs, topical or infiltration of local anaesthetic and regional techniques like sphenopalatine ganglion (SPG) block, infraorbital nerve block and nasociliary block. As the current evidences regarding the benefit of SPG block after FESS is controversial, efficacy of sphenopalatine ganglion block will be evaluated using bupivacaine or ropivacaine as local anaesthetic in adult patients undergoing FESS under general anaesthesia in this study.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Postgraduate Institute of Medical Education and ResearchTreatments:
Bupivacaine
Ropivacaine
Criteria
Inclusion Criteria:- 60 American Society of Anesthesiologists (ASA) physical status I and II patients
- aged 18-60 years scheduled to undergo elective functional endoscopic sinus surgery for
sinonasal disease such as rhinosinusitis, polyps and deviated nasal septum were
enrolled
Exclusion Criteria:
- Severe cardiovascular, pulmonary, hepatic, renal, neurologic or metabolic disease or
coagulopathy
- History of allergy to any of the medications being used in the study
- Previous surgery for sinonasal disease
- Pre-existing chronic pain not related to chronic rhinosinusitis
- Taking prescription pain medications or antidepressants
- Chronic alcohol or drug abuse
- Inability to comprehend the study protocol
- Pregnancy