Overview

Septorhinoplasty Post-operative Pain Control With SPG Nerve Block

Status:
Not yet recruiting
Trial end date:
2024-12-01
Target enrollment:
0
Participant gender:
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 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Florida
Treatments:
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