Evaluations of Optimizing Perioperative Fluid Management on Postoperative Pain Outcomes

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02245581

Enrollment

Registered

2014-09-19

Start date

2013-04-30

Completion date

Unknown

Last updated

2014-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients Major Laminectomy Surgery

Brief summary

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.

Interventions

PROCEDURESVV-guided fluid management

PROCEDURECVP-guided fluid management

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

20 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Pain at rest and movement	Post-operation Day1 to Day4

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026