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Use of Low-level Laser Therapy in the Treatment of Diabetic Foot Ulcers

Primary Purpose

Diabetic Foot Ulcer, Diabetic Foot

Status
Active
Phase
Phase 2
Locations
Brazil
Study Type
Interventional
Intervention
LG1
LG2
LG3
CC
Dressing
Sponsored by
Federal University of Piaui
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Foot Ulcer

Eligibility Criteria

18 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Type 2 diabetes mellitus patients with diabetic foot ulcers;
  • Patients aged 18 and over.

Exclusion Criteria:

  • Type 2 diabetes mellitus patients with ulcers in parts of the body other than the feet;
  • Patients with infected diabetic foot ulcers.

Sites / Locations

  • Federal University of Piaui

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

CC + dressing

LG1 + dressing

LG2 + dressing

LG3 + dressing

Arm Description

The group will receive placebo LASER application associated with Helianthus annuus oil dressing.

The group will receive application of LASER Gallium Arsenide (GaAs) 904 nm 10 J/cm² associated with Helianthus annuus oil dressing.

The group will receive application of LASER Gallium Arsenide (GaAs) 904 nm 8 J/cm² associated with Helianthus annuus oil dressing.

The group will receive application of LASER Gallium Arsenide (GaAs) 904 nm 4 J/cm² associated with Helianthus annuus oil dressing.

Outcomes

Primary Outcome Measures

Change in the ulcer area
Measure of ulcer area change.
Change in complete ulcer healing
Change in the percentage of complete ulcer healing.

Secondary Outcome Measures

Wagner Classification
Ulcer categorization according to Wagner Classification.
Blood glucose
Glycemic levels.
Temperature
Ulcer temperature.
Short Form-36 Health Survey questionnaire
The Short Form-36 Health Survey questionnaire (SF 36) assesses quality of life and consists of 36 questions, covering 8 domains. This questionnaire has a final score from 0 to 100, in which zero corresponds to the worst general health status and 100 to the best health status.

Full Information

First Posted
January 22, 2020
Last Updated
July 25, 2022
Sponsor
Federal University of Piaui
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1. Study Identification

Unique Protocol Identification Number
NCT04246814
Brief Title
Use of Low-level Laser Therapy in the Treatment of Diabetic Foot Ulcers
Official Title
Effect of Low-level Laser Therapy in the Treatment of Diabetic Foot Ulcers: a Double-blind Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 27, 2019 (Actual)
Primary Completion Date
August 18, 2021 (Actual)
Study Completion Date
December 18, 2022 (Anticipated)

3. Sponsor/Collaborators

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

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Diabetes mellitus (DM) is currently an important cause of morbidity and mortality. Global estimates indicate that 382 million people live with diabetes (8.3%), and that number could reach 592 million in 2035. The diabetic foot ulcers (DFU) present as sore wounds with disintegration of the skin. The DFU affect 15% of diabetic patients. Several studies have been conducted aiming to find therapeutic strategies for the healing of DFU, among the reported therapeutic methods the Low-level Laser Therapy (LLLT) has been highlighted. The aim of this study is to investigate the effects of different doses of LLLT in the treatment of DFU. Methods: This study is characterized as a double-blind randomized clinical trial (RCT), consisting of four groups, the control group will have only dressing and placebo LLLT application and the other three groups will have dressing and real LLLT GaAs 904 nm application. Expected outcomes: to elucidate the effects of different doses of LLLT GaAs 904 nm on the treatment of DFU, beyond to identify the most effective dose.
Detailed Description
All groups will perform the same procedures twice weekly. Volunteers will be comfortable with the affected foot exposed. The diabetic foot ulcers (DFU) will be cleaned using saline solution and gauze, then the ulcer temperature will be checked using the digital infrared thermometer. Diabetic wounds will be measured and photographed at baseline and every 10 visits until the study is completed, the images will be analyzed using the ImageJ program for follow-up throughout the intervention. The DFU will be ranked according to the Wagner Scale. Afterwards the volunteers will receive LLLT application and conventional treatment in the form of Helianthus Annuus oil dressing. Both therapist and participant will be instructed on precautions to be observed when using LLLT. Goggles will be provided prior to administration. The lower cylinder of the LASER probe will be placed perpendicular to the DFU, the floor and edges of the ulcer will be irradiated using punctual and scanning techniques, respectively. Once a week blood glucose levels will be obtained for patient screening. All data will be recorded until the end of the visits in a control form prepared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Foot Ulcer, Diabetic Foot

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
Masking will be double-blind, the volunteer and outcome assessor will not be aware of the individual allocation of participants in the intervention groups.
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CC + dressing
Arm Type
Placebo Comparator
Arm Description
The group will receive placebo LASER application associated with Helianthus annuus oil dressing.
Arm Title
LG1 + dressing
Arm Type
Active Comparator
Arm Description
The group will receive application of LASER Gallium Arsenide (GaAs) 904 nm 10 J/cm² associated with Helianthus annuus oil dressing.
Arm Title
LG2 + dressing
Arm Type
Active Comparator
Arm Description
The group will receive application of LASER Gallium Arsenide (GaAs) 904 nm 8 J/cm² associated with Helianthus annuus oil dressing.
Arm Title
LG3 + dressing
Arm Type
Active Comparator
Arm Description
The group will receive application of LASER Gallium Arsenide (GaAs) 904 nm 4 J/cm² associated with Helianthus annuus oil dressing.
Intervention Type
Device
Intervention Name(s)
LG1
Intervention Description
Application of LASER AsGa 904nm 10 J/cm².
Intervention Type
Device
Intervention Name(s)
LG2
Intervention Description
Application of LASER AsGa 904nm 8 J/cm².
Intervention Type
Device
Intervention Name(s)
LG3
Intervention Description
Application of LASER AsGa 904nm 4 J/cm².
Intervention Type
Device
Intervention Name(s)
CC
Intervention Description
Application of placebo LASER.
Intervention Type
Procedure
Intervention Name(s)
Dressing
Intervention Description
Application of Helianthus annuus oil dressing.
Primary Outcome Measure Information:
Title
Change in the ulcer area
Description
Measure of ulcer area change.
Time Frame
Before intervention starts, 5th and 10th week of intervention.
Title
Change in complete ulcer healing
Description
Change in the percentage of complete ulcer healing.
Time Frame
Before intervention starts, 5th and 10th week of intervention.
Secondary Outcome Measure Information:
Title
Wagner Classification
Description
Ulcer categorization according to Wagner Classification.
Time Frame
Before intervention starts, 5th and 10th week of intervention and after 1 month and after 1 month.
Title
Blood glucose
Description
Glycemic levels.
Time Frame
Before intervention starts, 5th and 10th week of intervention and after 1 month and after 1 month.
Title
Temperature
Description
Ulcer temperature.
Time Frame
Before intervention starts, 5th and 10th week of intervention.
Title
Short Form-36 Health Survey questionnaire
Description
The Short Form-36 Health Survey questionnaire (SF 36) assesses quality of life and consists of 36 questions, covering 8 domains. This questionnaire has a final score from 0 to 100, in which zero corresponds to the worst general health status and 100 to the best health status.
Time Frame
Before intervention starts, 5th and 10th week of intervention and after 1 month and after 1 month.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 2 diabetes mellitus patients with diabetic foot ulcers; Patients aged 18 and over. Exclusion Criteria: Type 2 diabetes mellitus patients with ulcers in parts of the body other than the feet; Patients with infected diabetic foot ulcers.
Facility Information:
Facility Name
Federal University of Piaui
City
Parnaíba
State/Province
Piauí
ZIP/Postal Code
64202-020
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34487920
Citation
Cardoso VS, de Souza Lima da Silveira PR, Dos Santos CM, da Rocha RB, Hazime FA. Dose-response and efficacy of low-level laser therapy on diabetic foot ulcers healing: Protocol of a randomized controlled trial. Contemp Clin Trials. 2021 Nov;110:106561. doi: 10.1016/j.cct.2021.106561. Epub 2021 Sep 4.
Results Reference
derived

Learn more about this trial

Use of Low-level Laser Therapy in the Treatment of Diabetic Foot Ulcers

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