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N/A N=63 Randomized Single-blind

Intraoperative Ocular Pressure in Lumbar Spine Fusion Patients

Raised Ocular Pressure

Enrolled (actual)
63
Serious AEs
0.0%
Results posted
Feb 2016
Primary outcome: Primary: Change in Intraoperative Ocular Pressure in Lumbar Spine Fusion Patients Head Raised 10 Degrees or Kept in Neutral Position — 9.26; 13.79 mm Hg

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Head raised 10 degrees (Procedure); Head in neutral position (Procedure)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
West Virginia University
Primary completion
Feb 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Intraoperative Ocular Pressure in Lumbar Spine Fusion Patients Head Raised 10 Degrees or Kept in Neutral Position
9.26; 13.79
SECONDARY
Change and Correlations in Intraoperative Ocular Pressure in Lumbar Spine Fusion Patients

Summary

A rare but terrible complication of vision loss has been known to occur after surgery, including spine surgery. It is commonly thought that increased intraocular pressure (IOP) is one of the reasons for this rare vision loss. It has been shown that the prone position can increase the IOP, and that tilting the patient with the head down can also increase IOP. The investigators will be measuring IOP before, during, and after a posterior spine surgery to see if the investigators can influence the intraocular pressure with elevated head position change. Two groups will be studied: one group of patients will receive standard care with the head in neutral position, while the other group will have the head slightly elevated 10 degrees during prone spine surgery.

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing elective lumbar spinal fusion surgery; ages 18-80

Exclusion Criteria

  • Less than 18 years of age
  • Glaucoma, previous eye surgery, eye injury, or eye trauma, cervical myelopathy, prior cervical spine surgery, current neoplasm, patients who have neck pain with 10 degrees active extension.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02342288). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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