Purpose

Observation study monitoring vital signs and anesthetic variables particularly heart rate during prospective, ocular manipulation and specifically uniform tension on extra ocular muscles during strabismus surgery. *IRB approval from 1992 covered in letter from then IRB chair Dr. Judith Whitcomb, Anchorage, Alaska (letter 10/2020).*

Conditions

Eligibility

Eligible Ages
Between 1 Month and 100 Years
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patient scheduled for ocular manipulation and tension on extra ocular muscles and strabismus surgery

Exclusion Criteria

  • anophthalmia

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
anticholinergic Patients who receive anticholinergic medication before strabismus surgery
  • Diagnostic Test: electrocardiograph
    electrocardiograph monitor during strabismus surgery
    Other names:
    • ECG, EKG
non-anticholinergic Patients who do not received anticholinergic medication before strabismus surgery
  • Diagnostic Test: electrocardiograph
    electrocardiograph monitor during strabismus surgery
    Other names:
    • ECG, EKG

Recruiting Locations

Alaska Children's EYE & Strabismus
Anchorage, Alaska 99508
Contact:
Robert W Arnold, MD
907-561-1917
pdimd@me.com

More Details

Status
Recruiting
Sponsor
Alaska Blind Child Discovery

Study Contact

Robert W Arnold, MD
907-242-6180
eyedoc@alaska.net

Detailed Description

Patients with ocular manipulation including those scheduled for strabismus surgery will have peri-operative variables monitored before, during and after uniform traction on extra ocular muscles (EOM). The oculocardiac reflex (OCR) will be elicited by quantified (200 gram, 10-second, square-wave) traction on Jameson muscle hook under insertion of an extra ocular muscle (EOM, rectus). Stable pre-tension heart rate, and greatest change heart rate will be recorded. Additional variables to be recorded: birthdate, gender, race, weight, iris color, pre-operative neurodevelopmental conditions, pre-operative medications, induction medications, expired carbon dioxide (CO2) levels, exhaled gas concentrations, anticholinergic medications, opioids, muscle relaxants, type of airway and the number of EOM operated.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.