Optimizing Postoperative Nutrition in Colorectal Surgery
NCT06737211
Bowel Ischemia, Colonic Diseases
Athens, Greece
View Trial DetailsNCT Number: NCT03284398
The primary study objective is to assess the rates of blood stream infection (BSI) from the use of Three-Chamber Bags (e.g., SmofKabiven®, Kabiven®, others) compared to Hospital Compounded Bags (HCBs) in patients requiring parenteral nutrition in Spanish hospitals.
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Notify Me18 year and older
All sexes
Observational
Hospital de Manacor, Manacor, Balearic Islands, Spain
This is a retrospective observational database study of patients receiving parenteral nutrition (PN) for at least 3 consecutive days with hospital admission date between January 1, 2013, and December 31, 2015 (study period).
The study will use an as treated approach, where patients will be followed from the index date (hospital admission day of the hospitalization during which PN is administered) up to patient discharge or death (observation period).
The study will be conducted using an initial EMR (Electronic Medical Record) data retrieval process, followed by manual data retrieval (chart review) that will complement data obtained from EMR. Data collection for manual data retrieval will be conducted through an eCRF.
The documentation of patient data will comprise two sequential steps. The initial step will include data of 30% of patients and then an interim analysis (IA) will be conducted. If IA shows positive results, data for the remaining 70% of patients (step II) will be gathered.
The study will be conducted in 10-14 sites in Spain.
Data analysis: Baseline demographics, co-morbidities, and hospitalization characteristics will be reported descriptively by means of mean with standard deviations and medians with ranges for continuous variables and by counts and percentages for categorical variables. Incidence rates for BSI will be reported by treatment group.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Entire study period, from January 1, 2013 and December 31, 2015
Confirmation of BSI required fulfillment of all of the following criteria:
Time frame: From date of admission to date of discharge
Percentage of patients presenting at least one episode of Sepsis during treatment with PN for each group (3CB vs HCB)
Time frame: Any day during PN treatment
Percentage of patients receiving antimicrobial agents during treatment with PN for each group (3CB vs HCB)
Time frame: Patients requiring vasopressor support at any time during treatment with PN
Percentages of patients requiring vasopressor support during PN treatment
Time frame: Patients requiring mechanical ventilation at any time during PN treatment
Percentage of patients requiring mechanical ventilation during PN treatment for each group (3CB vs HCB)
Time frame: Patients requiring renal replacement therapy for at least one day during PN treatment
Percentage of patients requiring Renal Replacement Therapy during PN treatment for each group (3CB vs HCB)
Time frame: During PN treatment inclusive day 1
Percentage of patients presenting newly-occurred abnormal laboratory results during PN for each group (3CB vs HCB)
Time frame: Any time during PN treatment
Percentage of patients presenting at least one organ failure during treatment with PN for each group (3CB vs HCB)
Time frame: Duration in days from admission to death or discharge for each treatment arm
Hospital length of stay in days for patients for each group (3CB vs HCB)
Time frame: All patients admitted in the ICU at any time during PN treatment
Total number of days in the ICU for each group (3CB vs HCB)
Fresenius Kabi
Industry
Observational Retrospective Analysis Assessing the Influence of Three-Chamber Bags Compared to Hospital Compounded Parenteral Nutrition Bags on Blood Stream Infections
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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.
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