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Clinical Trials/NCT03890510
NCT03890510CompletedNot Applicable

Effect of Different Fluid Volume on Ocular Parameters in Patients Undergoing Spine Surgery in Prone Position

Huashan Hospital1 site in 1 country97 target enrollmentStarted: May 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
97
Locations
1
Primary Endpoint
The change of intraocular pressure

Study Overview

Brief Summary

The purpose of this trial is to compare the effect of different fluid volume infusion on ocular parameters in patients undergoing spine surgery in prone position.

Detailed Description

In the prone position, the intraocular pressure and optic nerve sheath diameter increase progressively with time as compared with those in the supine position. Excessive fluid infusion may further increase intraocular pressure and optic nerve sheath diameter. Pulse pressure variation (PPV) is a dynamic index which can effectively assess fluid responsiveness during general anesthesia.Therefore,the investigators have designed a study to compare the effect of different fluid volume infusion guided by low and high PPV indices on intraocular pressure and optic nerve sheath of patients undergoing prone spine surgery with general anesthesia. One group of the patients will receive relatively loose fluid infusion (target value of PPV: 6%-9%),while the other group of the patients will receive limited fluid infusion (target value of PPV: 13%-16%).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Scheduled for elective spine surgery in prone position under general anesthesia
  • •American Society of Anesthesiologists (ASA) physical status I or II
  • •Have signed consent form

Exclusion Criteria

  • •History of eye disease or eye surgery
  • •Pregnancy or breast feeding
  • •Known Allergy to latex or Ringer's lactate solution
  • •Hyperlactacidemia,uncontrolled hypertension, diabetes mellitus, arrhythmia, cardiovascular disease,chronic pulmonary disease, swelling of any body part, abnormal of liver or renal function, anemia, etc.
  • •Body mass index(BMI)>30
  • •Expected operation time >6 hours
  • •Estimated Intraoperative hemorrhage >1000ml
  • •Taking part in other clinical trials in the last 3 months or at present

Arms & Interventions

Low PPV Group

Active Comparator

After anesthesia induction, patients will receive spine surgery under general anesthesia in the prone position. Ringer's lactate solution will be infused at 1ml/(kg·h ) as a basal speed. Ringer's lactate solution at a volume of 250ml will be used as a bolus dose. Repeat bolus doses will be given to maintain PPV at 6~9% when necessary. Intraoptic pressure and optic sheath diameter will be measured at multiple time points.

Intervention: Ringer's Lactate solution (Other)

Low PPV Group

Active Comparator

After anesthesia induction, patients will receive spine surgery under general anesthesia in the prone position. Ringer's lactate solution will be infused at 1ml/(kg·h ) as a basal speed. Ringer's lactate solution at a volume of 250ml will be used as a bolus dose. Repeat bolus doses will be given to maintain PPV at 6~9% when necessary. Intraoptic pressure and optic sheath diameter will be measured at multiple time points.

Intervention: Spine surgery under general Anesthesia in the prone position (Procedure)

High PPV Group

Active Comparator

After anesthesia induction, patients will receive spine surgery under general anesthesia in the prone position. Ringer's lactate solution will be infused at 1ml/(kg·h ) as a basal speed. Ringer's lactate solution at a volume of 250ml will be used as a bolus dose. Repeat bolus doses will be given to maintain PPV at 13~16% when necessary. Intraoptic pressure and optic sheath diameter will be measured at multiple time points.

Intervention: Ringer's Lactate solution (Other)

High PPV Group

Active Comparator

After anesthesia induction, patients will receive spine surgery under general anesthesia in the prone position. Ringer's lactate solution will be infused at 1ml/(kg·h ) as a basal speed. Ringer's lactate solution at a volume of 250ml will be used as a bolus dose. Repeat bolus doses will be given to maintain PPV at 13~16% when necessary. Intraoptic pressure and optic sheath diameter will be measured at multiple time points.

Intervention: Spine surgery under general Anesthesia in the prone position (Procedure)

Outcomes

Primary Outcomes

The change of intraocular pressure

Time Frame: 10min after anesthesia induction(supine1), 10min after prone position(prone1), 1 hour after the prone position(prone2), 2 hour after the prone position(prone3),at the end of the surgery(prone4), and 10min after return to the supine position(supine2).

Intraocular pressure will be measured with a TONO-PEN AVIA handheld tonometer.

Secondary Outcomes

  • The change of the optic sheath diameter(10min after anesthesia induction(supine1), 10min after prone position(prone1), 1 hour after the prone position(prone2), 2 hour after the prone position(prone3),at the end of the surgery(prone4), and 10min after return to the supine position(supine2).)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Xiao-Yu Yang, MD

Principal Investigator

Huashan Hospital

Study Sites (1)

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