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Completed

NCT Number: NCT03284398

Three-Chamber Bags Retrospective Study in Spain

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital de Manacor, Manacor, Balearic Islands, Spain

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About this study

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.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Adult hospital inpatients ≥ 18 years
  • Treatment with PN for at least 3 consecutive days
  • PN containing all three major macronutrients, delivered from 3CB or HCB
  • Patients with hospital admission between January 1, 2013, and December 31, 2015 (study period)

Exclusion criteria

  • Bloodstream infection before or at the same day of first PN administration
  • Immunosuppression due to concomitant therapy (e.g., immunosuppressive therapy due to transplantation, concomitant oral or intravenous administration of glucocorticoids) or disease (e.g., HIV, leukaemia)
  • Permanent vascular access (port, shunts for dialysis)
  • Femoral venous placement of central venous line used for PN
  • Burns, extensive skin injuries (e.g., Lyell´s disease)
  • Chemo-/radiotherapy for up to 3 months before hospital admission
  • Change of PN bag type during observation period, e.g., from HCBs to 3CBs or vice-versa

Treatment and study plan

Primary outcomes

  1. Percentage of Patients Presenting With a Confirmed Microbial Blood Stream Infection During Treatment With PN for Each Group (3CB vs HCB)

    Time frame: Entire study period, from January 1, 2013 and December 31, 2015

    Confirmation of BSI required fulfillment of all of the following criteria:

    • International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM) code for sepsis (038.x), septicemia (995.91), severe sepsis (995.92), septic shock (785.52), bacteremia (790.7), unspecified infection due to central venous catheter (999.31), or BSI due to central venous catheter (999.32)
    • Positive blood culture collected during PN administration
    • Concomitant antimicrobial therapy

Secondary outcomes

  1. Sepsis During PN

    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)

  2. Treatment With Antimicrobials During PN

    Time frame: Any day during PN treatment

    Percentage of patients receiving antimicrobial agents during treatment with PN for each group (3CB vs HCB)

  3. Use of Vasopressor Treatment

    Time frame: Patients requiring vasopressor support at any time during treatment with PN

    Percentages of patients requiring vasopressor support during PN treatment

  4. Use of Mechanical Ventilation

    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)

  5. Renal Replacement Therapy

    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)

  6. Newly-occurred Abnormal Laboratory Findings During PN

    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)

  7. Organ Failure

    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)

  8. Hospital Length of Stay (LOS)

    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)

  9. Length of Stay in the ICU

    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)

Sponsors and collaborators

Lead sponsor

Fresenius Kabi

Industry

Registry information

Official study title

Observational Retrospective Analysis Assessing the Influence of Three-Chamber Bags Compared to Hospital Compounded Parenteral Nutrition Bags on Blood Stream Infections

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Sep 15, 2017
Registry last updated
Jan 29, 2021

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.

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