Preoperative Nutritional Assessment for Predicting Complications Risk in Patients Undergoing Abdominal Surgery
NCT ID: NCT03719508
Last Updated: 2020-07-23
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
450 participants
OBSERVATIONAL
2013-01-05
2017-12-20
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.
Evaluation of Nutritional Scores as Predictive Factors of Postoperative Outcome After Pancreatic Surgery
NCT05608538
Malnutrition Assessment Tools in Surgery
NCT05393752
Comparison of Scoring Systems in Gastrointestinal Cancer Surgery
NCT07325656
The Effect of Preoperative Nutritional Assessment and Nutritional Support on Clinical Outcomes
NCT03115931
Preoperative Nutritional Assessment of The Patients Undergoing Major Gastrointestinal Surgery and Their Immediate Postoperative Outcome
NCT04039035
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The aim of the present study was to compare the prognostic power of different screening tools for post - op complications. This was a prospective observational cohort study, performed in patients scheduled for an abdominal operation in the Second Department of Surgery, Evangelismos General Hospital in Athens, Greece. All patients were screened at admission and before operation. Data were collected in a special form by the dietician and the surgeon, with the use of screening tools and the local Electronic Medical Record System called "Emrora". Patients were followed up after surgery until discharge by the surgeon who recorded any complication or case of death in a new form.
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.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Diseases of the digestive tract (oesophageal, gastric or intestinal), or other abdominal diseases requiring elective surgery,
Exclusion Criteria
* Pregnancy
* Major coagulopathy
* Permanent pacemaker
* Specific preoperative nutritional support before admission to hospital
* Unable to give consent
18 Years
80 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Evangelismos Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dimitrios Karayiannis
Clinical Dietitian, Department of Clinical Nutrition and Metabolism
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
George Stylianides, MD, PhD
Role: STUDY_DIRECTOR
2nd Department of Surgery
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Nutrition and Dietetics, Evaggelismos Hospital
Athens, Kolonaki, Greece
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.
23/27-01-2014
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.