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Doubleblinded RCT of the Omnilux on Lower Extremity Surgical Wounds Left to Heal by Second Intention

Primary Purpose

Wound

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Omnilux
Omnilux Sham
Sponsored by
University of Miami
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Wound focused on measuring wound, secondary intention healing, lower extremity

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Surgical defect on the lower extremity left to heal by secondary intention.
  • If women of child bearing potential, contraceptive measures should be used
  • Maximum size of wound is 5cm x5cm; there is no minimum size for the wound.

Exclusion Criteria:

  • History of porphyria photosensitive eruptions, diabetes mellitus, history of venous insufficiency, known history of peripheral arterial disease (ABI <0.8)
  • Use of any ointments or creams containing photosensitizers (coumarins or porphyrins) should be discontinued for 2 weeks prior
  • Use of systemic or local retinoids for the past 6 months.
  • Current pregnancy or breastfeeding
  • History of metastatic cancer.

Sites / Locations

  • University of Miami Hospital and Clinics/Sylvester Comprehensive Cancer Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Sham Group (Group 1)

Treatment group (Group 2)

Arm Description

This group will receive 4 sessions of Omnilux sham light, starting 1 week after the surgery. Frequency: 1 session every week (+/- 3 days), for 4 weeks. Session duration: 20 minutes

This group will receive 4 treatment sessions with Omnilux 633nm LED, starting 1 week after the surgery. Frequency: 1 session every week (+/- 3 days), for 4 weeks. Session duration: 20 minutes

Outcomes

Primary Outcome Measures

Number of Days Required for the Wound to Heal Completely
Assessment by the physician indicating wound closure

Secondary Outcome Measures

Change in Relative Area of the Surgical Wound Remaining
Initial area * ((total area in the evaluated week/total area in the first week) * 100) and reported as a percentage (%)
Change in Total Surface Area of the Surgical Wound
A blinded investigator manually outlines the wound using a digital planimetry device to measure the surface area in square centimeters.

Full Information

First Posted
February 27, 2015
Last Updated
May 2, 2019
Sponsor
University of Miami
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1. Study Identification

Unique Protocol Identification Number
NCT02383056
Brief Title
Doubleblinded RCT of the Omnilux on Lower Extremity Surgical Wounds Left to Heal by Second Intention
Official Title
Doubleblinded, Randomized, Controlled Trial to Study the Effect of Omnilux Light Emitting Diode on Wound Healing Following Lower Extremity Surgical Wounds Left to Heal by Second Intention
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Terminated
Why Stopped
Sufficient enrollment achieved for outcome measures
Study Start Date
December 2012 (undefined)
Primary Completion Date
November 2017 (Actual)
Study Completion Date
November 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Miami

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of the study is to evaluate the effectiveness of the light-emitting diode (LED) in promoting healing of the wound on lower leg as a result of surgery. Wounds on the lower leg heal more slowly than wounds on the head and neck; they can also remain deep red for six months to one year. Doctors usually allow a lower leg surgical wound to heal by itself, without stitches or other additional treatment. This is because leg wounds do not hold stitches well and stitches could cause other problems. A major drawback of allowing a surgical wound on the lower leg to heal by itself is the long healing time that can often take months. The investigators wish to evaluate if the LED light treatment of the surgical wound will improve the healing of your wound. In order to test if leg wounds heal faster after treatment with LED, half of the patients in the study will receive the LED (Group 2) and half will not receive treatment with LED but will receive a "sham light" treatment (Group 1). Essentially, a sham light treatment refers to regular light (not LED) exposure for 20 minutes. The sham light comes from the same device as the treatment light (Omnilux machine) however, this light has no anticipated effects on wound healing and is used simply to reduce the amount of bias that sometimes complicates the results of these studies. There is no added risk or benefit for the patients in the control group exposed to the sham light. Both groups will receive the standard care of wounds on the lower extremity.
Detailed Description
Group 2 of this study will receive the LED and half will not receive treatment with LED but will receive a "sham light" treatment (Group 1). Essentially, a sham light treatment refers to regular light (not LED) exposure for 20 minutes. The sham light comes from the same device as the treatment light (Omnilux machine) however, this light has no anticipated effects on wound healing and is used simply to reduce the amount of bias that sometimes complicates the results of these studies. There is no added risk or benefit for the patients in the control group exposed to the sham light. Both groups will receive the standard care of wounds on the lower extremity. Groups 1 and 2 will receive 4 sham light or treatment sessions, respectively (one session every week for 4 weeks). After these sessions are done, all subjects will continue weekly follow up visits until the wound is closed, or 3 months after the surgery have passed; which ever happens first. One final follow up visit will occur 1 week after the wound closed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wound
Keywords
wound, secondary intention healing, lower extremity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sham Group (Group 1)
Arm Type
Sham Comparator
Arm Description
This group will receive 4 sessions of Omnilux sham light, starting 1 week after the surgery. Frequency: 1 session every week (+/- 3 days), for 4 weeks. Session duration: 20 minutes
Arm Title
Treatment group (Group 2)
Arm Type
Experimental
Arm Description
This group will receive 4 treatment sessions with Omnilux 633nm LED, starting 1 week after the surgery. Frequency: 1 session every week (+/- 3 days), for 4 weeks. Session duration: 20 minutes
Intervention Type
Device
Intervention Name(s)
Omnilux
Intervention Description
Photomodulation irradiated with a 633 +/- 3 mm light source for 20 minutes (105 mW/cm, 126 J/cm)
Intervention Type
Device
Intervention Name(s)
Omnilux Sham
Intervention Description
Sham light instead of phototherapy from the same light device
Primary Outcome Measure Information:
Title
Number of Days Required for the Wound to Heal Completely
Description
Assessment by the physician indicating wound closure
Time Frame
84 days
Secondary Outcome Measure Information:
Title
Change in Relative Area of the Surgical Wound Remaining
Description
Initial area * ((total area in the evaluated week/total area in the first week) * 100) and reported as a percentage (%)
Time Frame
Week 1 to Week 2, Week 2 to Week 3, Week 3 to Week 4
Title
Change in Total Surface Area of the Surgical Wound
Description
A blinded investigator manually outlines the wound using a digital planimetry device to measure the surface area in square centimeters.
Time Frame
Week 1 to Week 2, Week 2 to Week 3, Week 3 to Week 4, Week 1 to Week 4

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: Surgical defect on the lower extremity left to heal by secondary intention. If women of child bearing potential, contraceptive measures should be used Maximum size of wound is 5cm x5cm; there is no minimum size for the wound. Exclusion Criteria: History of porphyria photosensitive eruptions, diabetes mellitus, history of venous insufficiency, known history of peripheral arterial disease (ABI <0.8) Use of any ointments or creams containing photosensitizers (coumarins or porphyrins) should be discontinued for 2 weeks prior Use of systemic or local retinoids for the past 6 months. Current pregnancy or breastfeeding History of metastatic cancer.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Keyvan Nouri, MD
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Miami Hospital and Clinics/Sylvester Comprehensive Cancer Center
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States

12. IPD Sharing Statement

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Doubleblinded RCT of the Omnilux on Lower Extremity Surgical Wounds Left to Heal by Second Intention

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