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Epidermal Grafting in Wound Healing (EPIGRAAFT)

Primary Purpose

Ulcer, Skin Ulcer, Wounds and Injuries

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Epidermal grafting
Split thickness skin grafting
Sponsored by
University College, London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcer focused on measuring epidermal graft, suction blister, blister graft, suction graft, Epidermis/su, tr [Surgery, Transplantation]

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Male or female
  2. Age 18-90
  3. Wound measuring more than 1cm x 1cm and lesser than 5cm x 5cm (1% TBSA)
  4. Wound with clean, healthy granulating bed, with minimal adherent slough
  5. Patient understands and is willing to participate and can comply with weekly visits and follow-up regime

Exclusion Criteria:

  1. Wound with active infection
  2. Wound at plantar of the foot
  3. Patients unsuitable for Split Skin Grafting
  4. Previous history of excessive bleeding associated with surgical biopsies or trauma
  5. Allergies to tegaderm (and other dressings used in the study)
  6. Known uncontrolled Diabetes Mellitus, as measured by an HbA1c > 10%.
  7. Presence of one or more medical conditions, including renal, hepatic, hematologic, active auto-immune or immune diseases that, would make the subject an inappropriate candidate for this ulcer healing study
  8. Patient not fit for surgery (ASA classification > 4)

Sites / Locations

  • Royal Free Hampstead NHS Trust Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Epidermal Graft

Split Thickness Skin Graft

Arm Description

The Cellutome Epidermal Graft Harvesting System will be used to harvest epidermal grafts as per existing normal clinical practice.

Split thickness skin graft will be harvested using air dermatome as per normal clinical practise.

Outcomes

Primary Outcome Measures

Number of Wounds With Complete Healing
Number of wounds with complete healing at 6 weeks
Mean Time for Donor Site Healing
Complete donor site healing was defined as 100% re-epithelialisation and not requiring further dressings

Secondary Outcome Measures

Time for Wound Healing
Complete wound healing was defined as 100% re-epithelialisation and not requiring further dressings
Donor Site Morbidity
The donor site morbidity was measured using the Vancouver Scar Scale (VSS). Total score scale ranges from 0 to 13. Lower score is more desirable as it represents a scar resembling normal surrounding skin. The scale assesses 4 categories: vascularity, height, pliability, and pigmentation. Total score is obtained by the sum of the categories.
Patient Reported Outcome Measure (PROM)
Patient reported outcome measure was assessed using a validated skin graft satisfaction questionnaire.The skin graft satisfaction questionnaire has a scale ranging from 1 to 7, with 1 representing very unsatisfied while 7 represents very satisfied. Hence, higher score represent higher satisfaction.
Adverse Events
Number of participants with of adverse events

Full Information

First Posted
August 11, 2015
Last Updated
July 24, 2020
Sponsor
University College, London
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1. Study Identification

Unique Protocol Identification Number
NCT02535481
Brief Title
Epidermal Grafting in Wound Healing
Acronym
EPIGRAAFT
Official Title
A Multi-centre Randomised Controlled Trial to Compare Epidermal Grafting With Split Skin Grafting for Wound Healing
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
October 2015 (Actual)
Primary Completion Date
August 2017 (Actual)
Study Completion Date
November 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University College, London

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Split thickness skin grafting is the normal standard of care for wound closure. However, this is an invasive procedure and associated with pain also there can be additional donor site morbidity. Epidermal grafting is an emerging clinical alternative that is gaining clinical practise. Epidermal grafting (EG) is an alternative method of autologous skin grafting that 'harvests' a finer layer of skin than traditional Split thickness skin grafting (SSG). This potentially results in less pain and reduced donor site morbidity but only delivers several cell layers to the wound so may be less effective at healing a wound. It is not known if EG is an effective alternative to SSG. Further the mechanism to achieve wound healing may be different. EG promotes wound healing by expressing growth factors that accelerates wound healing and encourages keratinocyte migration. Whereas SSG is a transplant of several skin layers that integrated to the existing wound bed as a formal skin covering. The investigators wish to compare these two clinical practises; epidermal grafting and split thickness skin grafting in wound healing. Further to undertake a translational study to investigate the mechanism by which each technique achieves wound healing.
Detailed Description
This study evaluates the efficacy of EG, as an alternative to current wound management therapy, SSG. In a pilot study carried out in our centre (unpublished data), the investigators noted that this technique offers a method of autologous skin harvesting with minimal or no pain and a scar free donor site. Moreover, complete wound epithelialisation was achieved while maintaining patient independence. Therefore, this device has the potential to save healthcare resources, by eliminating the need for theatre space and a hospital bed, and result in better Patient Reported Outcomes Measures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcer, Skin Ulcer, Wounds and Injuries
Keywords
epidermal graft, suction blister, blister graft, suction graft, Epidermis/su, tr [Surgery, Transplantation]

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Epidermal Graft
Arm Type
Experimental
Arm Description
The Cellutome Epidermal Graft Harvesting System will be used to harvest epidermal grafts as per existing normal clinical practice.
Arm Title
Split Thickness Skin Graft
Arm Type
Experimental
Arm Description
Split thickness skin graft will be harvested using air dermatome as per normal clinical practise.
Intervention Type
Device
Intervention Name(s)
Epidermal grafting
Other Intervention Name(s)
CelluTome
Intervention Description
The Cellutome Epidermal Graft Harvesting System will be used to harvest epidermal grafts.
Intervention Type
Procedure
Intervention Name(s)
Split thickness skin grafting
Intervention Description
Split thickness skin grafting will be performed as per normal clinical practice.
Primary Outcome Measure Information:
Title
Number of Wounds With Complete Healing
Description
Number of wounds with complete healing at 6 weeks
Time Frame
6 weeks and 3 months
Title
Mean Time for Donor Site Healing
Description
Complete donor site healing was defined as 100% re-epithelialisation and not requiring further dressings
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Time for Wound Healing
Description
Complete wound healing was defined as 100% re-epithelialisation and not requiring further dressings
Time Frame
3 months
Title
Donor Site Morbidity
Description
The donor site morbidity was measured using the Vancouver Scar Scale (VSS). Total score scale ranges from 0 to 13. Lower score is more desirable as it represents a scar resembling normal surrounding skin. The scale assesses 4 categories: vascularity, height, pliability, and pigmentation. Total score is obtained by the sum of the categories.
Time Frame
6 weeks and 3 months
Title
Patient Reported Outcome Measure (PROM)
Description
Patient reported outcome measure was assessed using a validated skin graft satisfaction questionnaire.The skin graft satisfaction questionnaire has a scale ranging from 1 to 7, with 1 representing very unsatisfied while 7 represents very satisfied. Hence, higher score represent higher satisfaction.
Time Frame
6 weeks and 3 months
Title
Adverse Events
Description
Number of participants with of adverse events
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male or female Age 18-90 Wound measuring more than 1cm x 1cm and lesser than 5cm x 5cm (1% TBSA) Wound with clean, healthy granulating bed, with minimal adherent slough Patient understands and is willing to participate and can comply with weekly visits and follow-up regime Exclusion Criteria: Wound with active infection Wound at plantar of the foot Patients unsuitable for Split Skin Grafting Previous history of excessive bleeding associated with surgical biopsies or trauma Allergies to tegaderm (and other dressings used in the study) Known uncontrolled Diabetes Mellitus, as measured by an HbA1c > 10%. Presence of one or more medical conditions, including renal, hepatic, hematologic, active auto-immune or immune diseases that, would make the subject an inappropriate candidate for this ulcer healing study Patient not fit for surgery (ASA classification > 4)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Toby Richards, MD FRCS
Organizational Affiliation
University College, London
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Afshin Mosahebi, MBBS FRCS PhD MBA
Organizational Affiliation
Royal Free Hospital NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Free Hampstead NHS Trust Hospital
City
London
ZIP/Postal Code
NW3 2QG
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
32532631
Citation
Kanapathy M, Bystrzonowski N, Hachach-Haram N, Twyman L, Becker DL, Richards T, Mosahebi A. Lower donor site morbidity and higher patient satisfaction with epidermal grafting in comparison to split thickness skin grafting: A randomized controlled trial (EPIGRAAFT Trial). J Plast Reconstr Aesthet Surg. 2020 Aug;73(8):1556-1564. doi: 10.1016/j.bjps.2020.03.006. Epub 2020 Mar 16.
Results Reference
derived
PubMed Identifier
27185033
Citation
Kanapathy M, Hachach-Haram N, Bystrzonowski N, Harding K, Mosahebi A, Richards T. Epidermal grafting versus split-thickness skin grafting for wound healing (EPIGRAAFT): study protocol for a randomised controlled trial. Trials. 2016 May 17;17(1):245. doi: 10.1186/s13063-016-1352-y.
Results Reference
derived

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Epidermal Grafting in Wound Healing

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