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OpenTrials
Completed

NCT Number: NCT02245581

Evaluations of Optimizing Perioperative Fluid Management on Postoperative Pain Outcomes

Patient characteristics, duration of surgery, and infusion volumes will be compared between the groups. Oxygen transport and organ function will be compared Length of hospital stay, morbidity, postoperative pain intensity were compared. Continuous variables will be analyzed using the student t-test and discrete variables will be analyzed using Chi-Square test. P-value <0.05 will be considered significant, where appropriate 95% confidence intervals will be calculated. Statistical analysis will be carried out using standardize statistical programs SPSS 12.0 for windows.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kaohsiung Veterans General Hospital

Kaohsiung City, 81362, Taiwan

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients are undergoing elective spine laminectomy

Exclusion criteria

  • age <20 yr
  • emergency surgery
  • coagulopathy
  • renal and hepatic dysfunction
  • hyperthyroidism, and cardiac rhythm other than sinus rhythm

Treatment and study plan

SVV-guided fluid management

Procedure

CVP-guided fluid management

Procedure

Primary outcomes

  1. Pain at rest and movement

    Time frame: Post-operation Day1 to Day4

Sponsors and collaborators

Lead sponsor

Kaohsiung Veterans General Hospital.

Other

Registry information

Important dates

Study start
2013
Primary completion
2014
First posted
Sep 19, 2014
Registry last updated
Sep 19, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.