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The Effect of a Local Injection of a Platelet Concentrate on Infection and Healing of Surgical Wounds

Primary Purpose

Wound Infection and Wound Healing

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Leucocyte - Platelet rich Plasma
Vitamin C
Zinc
L-Arginine
Sponsored by
Jens Rikardt Andersen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Wound Infection and Wound Healing

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient at Rigshospitalets Surgical gastroenterology clinic
  • Planned to have a Pancreaticoduodenectomy preformed
  • Being able to understand Danish, the trial and what it means to be enrolled in the trial
  • Capable of signing a written consent
  • Living i the Regional Capital (excl. Bornholm) or the Regional of Sjælland (north of Næstved)

Exclusion Criteria:

  • Dysregulated diabetes mellitus type I or II
  • Alcohol consumption above 14 or 7 x 12 g alcohol per week (men vs women)
  • Participating in another clinical trial

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Leucocyte - Platelet rich Plasma and Dietary Supplements

    Treatment as usual

    Arm Description

    An application of an autologous platelet concentrate (20 ml). This is injected once, locally in the muscle after closure of the inner fascia and before closure of the outer fascia. A daily dietary supplement of Vitamin C, Zinc and L-Arginine. Provided from POD2-3 until POD30

    Patients are treated as usual.

    Outcomes

    Primary Outcome Measures

    Number of patients with wound infection assessed by traditional clinical observation of the cicatrice
    Infection are defined as a collection of pus in the wound that require revision. It is assessed by observation from the hospital staff.

    Secondary Outcome Measures

    Number of days before the surgical wound are full epithelized assessed by observation of the cicatrice
    Digital photos of the cicatrice will be collected and analyzed for the amount of remaining scab.
    Other postoperative complications
    Length of stay (LOS)
    Experience of pain assessed by a VAS (Visual analogue scale)
    Mobilization assessed by "Timed Up & Go (TUG)"
    Timed Up & Go, also known as TUG, measures the time it takes a study subject to stand up, walk 3 meters, turn around, walk back and sit down.
    Inflammatory responds assessed by blood sample analysis of the acute phase reactant CRP (c-reactive protein)
    Inflammatory responds assessed by blood sample analysis of the acute phase reactant leucucytes

    Full Information

    First Posted
    August 3, 2016
    Last Updated
    August 11, 2016
    Sponsor
    Jens Rikardt Andersen
    Collaborators
    Rigshospitalet, Denmark
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02869204
    Brief Title
    The Effect of a Local Injection of a Platelet Concentrate on Infection and Healing of Surgical Wounds
    Official Title
    The Effect of L-PRP on Wound Healing and Wound Infection After Pancreaticoduodenectomy / Whipples Surgery
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2016
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 2016 (undefined)
    Primary Completion Date
    February 2017 (Anticipated)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Jens Rikardt Andersen
    Collaborators
    Rigshospitalet, Denmark

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this project is to investigate whether a combination of a local injection of platelet rich plasma (PRP) combined with a daily supplement of vitamin C, zinc, L-arginine, as well as high protein diet (1.5 g of protein per kilo body weight per day) can promote tissue healing in patients undergoing open upper-abdominal surgery. Primary endpoint is cases of wound infection and secondary endpoints are time of tissue regeneration (days), judged by traditional clinical observation and experimentally assessed by ultrasound. The experiment is performed as a parallel two-armed, randomized, controlled trial. A total of 40 subjects will be included in the trial i order to ensure the power of the study, despite a drop off of up to 25%.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Wound Infection and Wound Healing

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    40 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Leucocyte - Platelet rich Plasma and Dietary Supplements
    Arm Type
    Experimental
    Arm Description
    An application of an autologous platelet concentrate (20 ml). This is injected once, locally in the muscle after closure of the inner fascia and before closure of the outer fascia. A daily dietary supplement of Vitamin C, Zinc and L-Arginine. Provided from POD2-3 until POD30
    Arm Title
    Treatment as usual
    Arm Type
    No Intervention
    Arm Description
    Patients are treated as usual.
    Intervention Type
    Other
    Intervention Name(s)
    Leucocyte - Platelet rich Plasma
    Other Intervention Name(s)
    L-PRP
    Intervention Description
    Autologous L-PRP are studied regarding it's accelerating effect on tissue repair.
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Vitamin C
    Intervention Description
    A daily dietary supplement of 500 mg Vitamin C. Provided from POD2-3 until POD30
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Zinc
    Intervention Description
    A daily dietary supplement of 44 mg Zinc. Provided from POD2-3 until POD30
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    L-Arginine
    Intervention Description
    A daily dietary supplement of 5 g L-Arginine. Provided from POD2-3 until POD30
    Primary Outcome Measure Information:
    Title
    Number of patients with wound infection assessed by traditional clinical observation of the cicatrice
    Description
    Infection are defined as a collection of pus in the wound that require revision. It is assessed by observation from the hospital staff.
    Time Frame
    From date of surgery until the date of first documented event of infection or date of death from any cause, whichever came first, assessed up to 30 days .
    Secondary Outcome Measure Information:
    Title
    Number of days before the surgical wound are full epithelized assessed by observation of the cicatrice
    Description
    Digital photos of the cicatrice will be collected and analyzed for the amount of remaining scab.
    Time Frame
    Up to 30 days
    Title
    Other postoperative complications
    Time Frame
    Up to 30 days
    Title
    Length of stay (LOS)
    Time Frame
    30 days
    Title
    Experience of pain assessed by a VAS (Visual analogue scale)
    Time Frame
    Up to 30 days
    Title
    Mobilization assessed by "Timed Up & Go (TUG)"
    Description
    Timed Up & Go, also known as TUG, measures the time it takes a study subject to stand up, walk 3 meters, turn around, walk back and sit down.
    Time Frame
    Up to 30 days
    Title
    Inflammatory responds assessed by blood sample analysis of the acute phase reactant CRP (c-reactive protein)
    Time Frame
    Up to 30 days
    Title
    Inflammatory responds assessed by blood sample analysis of the acute phase reactant leucucytes
    Time Frame
    Up to 30 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patient at Rigshospitalets Surgical gastroenterology clinic Planned to have a Pancreaticoduodenectomy preformed Being able to understand Danish, the trial and what it means to be enrolled in the trial Capable of signing a written consent Living i the Regional Capital (excl. Bornholm) or the Regional of Sjælland (north of Næstved) Exclusion Criteria: Dysregulated diabetes mellitus type I or II Alcohol consumption above 14 or 7 x 12 g alcohol per week (men vs women) Participating in another clinical trial

    12. IPD Sharing Statement

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    The Effect of a Local Injection of a Platelet Concentrate on Infection and Healing of Surgical Wounds

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