Overview
Septorhinoplasty Post-operative Pain Control With SPG Nerve Block
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2024-12-01
2024-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
Maxillary nerve blocks have been shown to significantly reduce post-operative pain and analgesic intake during the 24-hour period following sinus surgery. This randomized, double-blinded, placebo-controlled study will investigate blocks of the pterygopalatine fossa using a suprazygomatic approach during septorhinoplasty surgery. It is the investigator's hypothesis that this technique will result in decreased post-operative pain and opioid use, and the morbidity associated with it.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
University of FloridaTreatments:
Dexamethasone
Ropivacaine
Criteria
Inclusion Criteria:- Patient presenting for open or endoscopic septorhinoplasty
- Age 18-80
- Normal oral food and water intake before surgery
- ASA physical classification 1-3
Exclusion Criteria:
- Refusal to consent
- Patients without a cellular phone or who are unable to accept text messages
- Allergy to opioid narcotics
- ASA physical classification of 4 or higher
- Patient requires other surgery in addition to septorhinoplasty
- Age > 80 or <18
- Any underlying chronic pain condition or ongoing opioid use over the preceding 3
months
- Presence of any other factor which, at the discretion of any member of the study team,
makes the patient a poor candidate for block placement.
- Presence of any other factor which, at the discretion of any member of the study team,
makes the patient a poor candidate for research participation.
- Pregnant women