Evaluations of Optimizing Perioperative Fluid Management on Postoperative Pain Outcomes
NCT ID: NCT02245581
Last Updated: 2014-09-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
72 participants
INTERVENTIONAL
2013-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Goal-directed Intraoperative Fluid Therapy in High-risk Surgery
NCT02470221
Implication of Fluid Strategies Upon Hepatic Outcome in Hepatobiliary Surgery
NCT03923816
Stroke Volume Variation-guided Fluid Infusion in Major Liver Tumour Resection
NCT05361252
Fluid Management Strategies on Blood Loss in Liver Transplantation
NCT06215404
Evaluation of Goal-Directed Intraoperative Hemodynamic Optimization Protocol
NCT02057653
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
SVV-guided fluid management
SVV : Stoke volume variation
SVV-guided fluid management
CVP-guided fluid management
CVP : Central venous pressure
CVP-guided fluid management
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
SVV-guided fluid management
CVP-guided fluid management
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* emergency surgery
* coagulopathy
* renal and hepatic dysfunction
* hyperthyroidism, and cardiac rhythm other than sinus rhythm
20 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Kaohsiung Veterans General Hospital.
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yuan-Yi Chia
anesthesia doctor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kaohsiung Veterans General Hospital
Kaohsiung City, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
VGHKS-102-036
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.