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The Effect of High vs. Low Fluid Volume on Ocular Parameters in Prone Spine Surgery

NCT03890510 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 97

Last updated 2020-12-17

No results posted yet for this study

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.

Conditions

  • Prone Position
  • Blood Volume
  • Intraocular Pressure

Interventions

OTHER

Ringer's Lactate solution

Patients in both groups will receive Ringer's lactate solution continuously during operation with different infusion volume.

PROCEDURE

Spine surgery under general Anesthesia in the prone position

The surgery, general anesthesia, and the placement of the prone position will be performed according to the standard procedures.

Sponsors & Collaborators

  • Huashan Hospital

    lead OTHER

Principal Investigators

  • Xiaoyu Yang, M.D. · Huashan Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-01
Primary Completion
2020-08-31
Completion
2020-09-07

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03890510 on ClinicalTrials.gov