Strabismus Recovery With Proparacaine and Oculocardiac Reflex
Completed
- Conditions
- BradycardiaPainNauseaStrabismus
- Interventions
- Drug: Topical Solution
- Registration Number
- NCT03672435
- Lead Sponsor
- Alaska Blind Child Discovery
- Brief Summary
Observational study to determine if topical anesthetic and intraoperative oculocardiac reflex influence post strabismus surgery recovery.
- Detailed Description
In an observational study with de-identified data of oculocardiac reflex (OCR) and strabismus surgery under routine anesthesia, a cohort of ongoing patients received topical proparacaine immediately post op, or none. Co-variables were intraoperative opioid and OCR, patient age, type of surgery. Several post-operative recovery outcome variables were prospectively monitored.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 140
Inclusion Criteria
- Strabismus surgery
Exclusion Criteria
- none
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description proparacaine Topical Solution Received topical proparacaine 0.5% with routine antibiotic-steroid ointment in operative eye(s) following strabismus surgery
- Primary Outcome Measures
Name Time Method pain (post op pain Likert scale) hours (1-4) in recovery room pain scale description / observation.. Pain is ranked by patient or nurse from 0 (no pain) to 9 (much pain)
- Secondary Outcome Measures
Name Time Method nausea hours (1-4) in recovery room observed or described nausea (presence or absence of nausea / vomiting)
heart rate hours (1-4) while in recovery room recovery room heart rate
time to recovery minutes (30-240) from entry recovery room to discharge time in recovery room