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
About this trial
This is an interventional prevention trial for Wound Infection and Wound Healing
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
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
NCT ID
NCT02869204
First Posted
August 3, 2016
Last Updated
August 11, 2016
Sponsor
Jens Rikardt Andersen
Collaborators
Rigshospitalet, Denmark
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
Learn more about this trial
The Effect of a Local Injection of a Platelet Concentrate on Infection and Healing of Surgical Wounds
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