The Efficacy of "MediHoney" to Facilitate Catheter Exit-Site Surgical Wound Healing
Primary Purpose
Renal Failure
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MediHoney
Sponsored by
About this trial
This is an interventional treatment trial for Renal Failure
Eligibility Criteria
Inclusion Criteria:
- Patients requiring dialysis due to loss of kidney function
- Patients choosing Peritoneal Dialysis (PD) for treatment
- All PD patients having an indwelling PD catheter placed
Exclusion Criteria:
- Patients younger than 18 years of age
- Prisoners
- Patients with mental defect
- Veteran Administration patients
Sites / Locations
- University of Missouri Department of Medicine; Dialysis Clinic, Inc.
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Standard Care
MediHoney
Arm Description
This group will undergo the current standard of care for post operative exit sites at the involved institutions. This group will act as the control or the group to which the interventional group will be compared too.
This study group will have the dry 2 x 2 dressing replaced with a honey 2 x 2 dressing. Additionally all indentations in the exit site wound will be filled with honey ointment prior to the application of the dressing.
Outcomes
Primary Outcome Measures
Time From Catheter Implantation to First Exit Site Infection.
The outcome measure is the length of time from implantation until the patient has first exit site infection or two years which ever is shortest.
Secondary Outcome Measures
Full Information
NCT ID
NCT01230489
First Posted
October 27, 2010
Last Updated
July 19, 2018
Sponsor
University of Missouri-Columbia
Collaborators
Dialysis Clinic, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT01230489
Brief Title
The Efficacy of "MediHoney" to Facilitate Catheter Exit-Site Surgical Wound Healing
Official Title
The Efficacy of "MediHoney" to Facilitate Catheter Exit-Site Surgical Wound Healing and Prevention of Wound Bacterial Colonization: A Randomized, Open-label, Controlled, Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Terminated
Why Stopped
Breakdown of communication between departments involved
Study Start Date
January 2011 (Actual)
Primary Completion Date
November 28, 2016 (Actual)
Study Completion Date
November 28, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Missouri-Columbia
Collaborators
Dialysis Clinic, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
To evaluate the efficacy of honey as a post surgical exit site care process to promote healing and prevent infectious bacterial colonization of newly created exit sites. It has been shown in the medical literature that honey has properties that are conducive to healing and the prevention of infection. In one study it was demonstrated that in urethral injury in the rat treated with honey the injury healed with none of the usual formation of fibrous tissue seen in such healing processes, that there was no reduction in the luminal diameter usually seen, and that the cells lining the urethra were uncompromised in any way, i.e. totally normal and healthy. We feel that if an exit site can be healed quickly with good normal tissue being developed that the patient will have a much better chance to keep that exit healthy reducing time, cost, and disruption of lifestyle. Other positive aspects of honey are it has the low pH required for good healthy tissue healing, it works in the presence of wound fluids, and it has never been shown to produce a resistant bacterial strain.
Detailed Description
The exit site (ES) of any transcutaneous device, or foreign body, through the skin presents as the site most vulnerable in terms of device survival. With the large numbers of catheters in use in chronic dialysis today exit-site care for the prevention of infection is of critical importance in reducing morbidity and mortality. Pericatheter infection is the number one cause of catheter loss in peritoneal dialysis patients.
It appears that honey is a compound with a multi-factorial mode of action. It is thought that with most honeys, the antimicrobial action stems from its high osmolality and the fact that it produces continuous non-cytotoxic levels of hydrogen peroxide due to enzymatic break down of the sugar. Honey also has a low pH which is not conducive for most bacterial growth but is good for wound healing.
Observational reports have shown some success in healing infected wounds, ulcers, protection of plastic surgery transplants, burns, herpetic skin lesions, and atopic dermatitis. Honey has also been shown to have antimicrobial action against a broad spectrum of fungi and bacteria including antibiotic resistant bacteria. Another study reports that honey reduces inflammation, edema, and promotes angiogenesis.
In an animal study of urethral injury it was shown that contrary to controls, there was a total healing with restoration of normal urethral epithelium and connective tissue with complete absence of fibrosis and inflammation. There was also no narrowing of the lumen as seen in the other study groups.
A study of prophylactic exit-site care of hemodialysis catheters comparing honey and Mupirocin demonstrated that results with honey were comparable to that of Mupirocin. However, unlike Mupirocin, there has not been an emergence of honey-resistant bacterial strains which makes it an attractive alternative agent.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Failure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
13 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Standard Care
Arm Type
No Intervention
Arm Description
This group will undergo the current standard of care for post operative exit sites at the involved institutions. This group will act as the control or the group to which the interventional group will be compared too.
Arm Title
MediHoney
Arm Type
Experimental
Arm Description
This study group will have the dry 2 x 2 dressing replaced with a honey 2 x 2 dressing. Additionally all indentations in the exit site wound will be filled with honey ointment prior to the application of the dressing.
Intervention Type
Biological
Intervention Name(s)
MediHoney
Other Intervention Name(s)
Honeycolloid Dressing, Leptospermum honey
Intervention Description
In this group a Medihoney 2 x 2 will be used in place of the standard dry 2 x 2 currently used as the wound dressing. Also all indentations of the wound will be filled with Medi-Honey ointment prior to the application of the dressing.
Primary Outcome Measure Information:
Title
Time From Catheter Implantation to First Exit Site Infection.
Description
The outcome measure is the length of time from implantation until the patient has first exit site infection or two years which ever is shortest.
Time Frame
Two years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients requiring dialysis due to loss of kidney function
Patients choosing Peritoneal Dialysis (PD) for treatment
All PD patients having an indwelling PD catheter placed
Exclusion Criteria:
Patients younger than 18 years of age
Prisoners
Patients with mental defect
Veteran Administration patients
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harold L Moore, MA
Organizational Affiliation
University of Missouri, School of Medicine, Department of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Missouri Department of Medicine; Dialysis Clinic, Inc.
City
Columbia
State/Province
Missouri
ZIP/Postal Code
65201
Country
United States
12. IPD Sharing Statement
Learn more about this trial
The Efficacy of "MediHoney" to Facilitate Catheter Exit-Site Surgical Wound Healing
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