search
Back to results

Hyperbaric Oxygen Therapy (HBOT) for Chronic Diabetic Lower Limb Ulcers (HBOT)

Primary Purpose

Diabetes Mellitus, Chronic Ulcers of the Lower Limb

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Hyperbaric Oxygen Therapy
Placebo Hyperbaric Oxygen Chamber
Sponsored by
St. Joseph's Healthcare Hamilton
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus focused on measuring Chronic ulcers, Diabetes, Hyperbaric Oxygen Therapy

Eligibility Criteria

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

Inclusion Criteria:

  • Age > 18 years
  • Type 1 or 2 Diabetes Mellitus
  • Wagner grading of foot lesions 3 or 4 on lower limb not healing for 4 weeks.

Exclusion Criteria:

  • Impending urgent amputation due to ongoing or exacerbated infection;
  • Exposed calcaneus bone with no prospect of weight bearing potential even if defect has been healed;
  • Dialysis-dependent renal failure;
  • Any of the following medical conditions which preclude safe treatment in a monoplace chamber: clinical depression; severe dementia; claustrophobia; seizure disorder; active asthma; severe chronic obstructive pulmonary disease; previous thoracic surgery; previous spontaneous or trauma induced pneumothorax; history of severe congestive heart failure with left ventricular ejection fraction less than 20%; unstable angina; chronic sinusitis; chronic or acute otitis media or major ear drum trauma; severe kyphoscoliosis; arthritis; or morbid obesity;
  • History of chemotherapy with use of Bleomycin;
  • Participation in another investigative drug or device trial currently or within the last 30 days;
  • Current candidates for vascular surgery, angioplasty or stenting;
  • Major large vessel disease;
  • Undergone vascular surgery or angioplasty within the last 3 months;
  • Women who are currently pregnant or are breast feeding or women of childbearing potential who are not currently taking adequate birth control.

Sites / Locations

  • Judy Dan Wound Care Centre/University Health Network

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

1

2

Arm Description

Hyperbaric Oxygen Therapy

Placebo Hyperbaric Oxygen Chamber

Outcomes

Primary Outcome Measures

Freedom from having, or meeting the criteria for, a major amputation (below knee amputation, or metatarsal level) up to 12 weeks after randomization.

Secondary Outcome Measures

Wound healing: difference in wound measurements (i.e. depth, length, width and extent of surface area); reduction in Wagner Classification Score; proportion of wound closed at 12 weeks of any time interval prior to end point; time to healing (days)
Effectiveness: maintenance on therapy (discontinuation rates); and secondary prevention interventions (confounding variables that may influence primary outcome such as diabetes control)
Safety: Major morbidity (infection requiring hospitalization, renal failure); wound interventions during study (debridement, surgery); Complications related to HBOT (seizure, pulmonary syndromes, vision disturbance; and all cause mortality
Healthcare resource utilization: wound dressing materials; healthcare provider visits; inpatient hospital admissions; complex continuing care/rehabilitation; drug therapy; mobility assistive devices
Quality of life: assessed by Standard Form 36 (SF-36) domain scores; EuroQoL 5D (EQ-5D) summary scores and by the Diabetic Foot Ulcer-Short Form (DFS-SF) scores
Cost effectiveness of HBOT: calculate the incremental cost per amputation avoided and the incremental cost per quality-adjusted life-year (QALY) gained

Full Information

First Posted
January 29, 2008
Last Updated
May 7, 2013
Sponsor
St. Joseph's Healthcare Hamilton
Collaborators
Judy Dan Research and Treatment Centre Ontario Wound Care Inc, University Health Network, Toronto
search

1. Study Identification

Unique Protocol Identification Number
NCT00621608
Brief Title
Hyperbaric Oxygen Therapy (HBOT) for Chronic Diabetic Lower Limb Ulcers
Acronym
HBOT
Official Title
A Prospective, Double-blind, Randomized, Controlled Clinical Trial Comparing Standard Wound Care With Adjunctive Hyperbaric Oxygen Therapy (HBOT) to Standard Wound Care Only for the Treatment of Chronic, Non-healing Ulcers of the Lower Limb in Patients With Diabetes Mellitus.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2013
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
April 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Joseph's Healthcare Hamilton
Collaborators
Judy Dan Research and Treatment Centre Ontario Wound Care Inc, University Health Network, Toronto

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine if HBOT plus standard wound care is more effective than standard wound care alone at preventing the need for major amputation (metatarsal and up) in patients with diabetes mellitus (Type 1 or 2) with moderate to sever chronic wounds of lower limbs.
Detailed Description
People with diabetes mellitus and non-healing ulcers of the lower limb are at higher risk of amputation. Current standard care for foot ulcers includes maintaining optimal blood glucose levels, use of debridement, antibacterials, dressings, antibiotics for infection; adequate nutrition; pressure relief and amputation. There has been an increased interest in the use of hyperbaric oxygen therapy (HBOT) as an adjunctive treatment for diabetic ulcers. HBOT is an established technology which currently is an accepted treatment of chronic diabetic ulcers in Ontario and physicians who provide this service are reimbursed under the current Ontario Health Insurance Plan (OHIP). However there are only a few facilities that can provide this service. In addition, results of published HBOT studies are inconsistent. The current study will provide quality efficacy data on the use of HBOT as an adjunctive therapy. As this study has been recommended by the Ontario Health Technology Advisory Committee (OHTAC), the results of the study will be used to make policy decisions regarding the funding and further utilization of HBOT therapy for people with diabetes mellitus with ulcers of the lower limb in the province. If the results are favorable towards HBOT in the treatment of diabetic ulcers, potential expansion and availability of this and other programs maybe be possible. A randomized placebo control trial evaluating HBOT, to the best of our knowledge has not been completed in this area and will provide much needed information to the scientific community.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Chronic Ulcers of the Lower Limb
Keywords
Chronic ulcers, Diabetes, Hyperbaric Oxygen Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
107 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Hyperbaric Oxygen Therapy
Arm Title
2
Arm Type
Sham Comparator
Arm Description
Placebo Hyperbaric Oxygen Chamber
Intervention Type
Procedure
Intervention Name(s)
Hyperbaric Oxygen Therapy
Intervention Description
Hyperbaric Oxygen Therapy (HBOT) will be provided 5 days per week for 6 weeks for a total of 30 treatments on average. Subjects will be placed into the hyperbaric chamber for approximately 90 minutes of HBOT at 2.4 ATA (partial pressure of oxygen = 1,800 mmHg) when inside the chamber. Subjects will receive dressing changes as required per standard of care.
Intervention Type
Procedure
Intervention Name(s)
Placebo Hyperbaric Oxygen Chamber
Intervention Description
Patients will receive HBOT placebo 5 days per week for 6 weeks for a total of 30 treatments. Each patient will be placed into the hyperbaric chamber and will receive 90 minutes of room air while inside the chamber and the initial flow of air into the chamber will produce a small increase in pressure (0.3 ATA partial pressure of oxygen = 210 mmHg) which will then be released over a period of 10 minutes. Subjects will receive dressings changes as required per standard of care.
Primary Outcome Measure Information:
Title
Freedom from having, or meeting the criteria for, a major amputation (below knee amputation, or metatarsal level) up to 12 weeks after randomization.
Time Frame
up to 12 weeks after randomization
Secondary Outcome Measure Information:
Title
Wound healing: difference in wound measurements (i.e. depth, length, width and extent of surface area); reduction in Wagner Classification Score; proportion of wound closed at 12 weeks of any time interval prior to end point; time to healing (days)
Time Frame
up to 12 weeks after randomization
Title
Effectiveness: maintenance on therapy (discontinuation rates); and secondary prevention interventions (confounding variables that may influence primary outcome such as diabetes control)
Time Frame
up to 12 weeks after Randomziation
Title
Safety: Major morbidity (infection requiring hospitalization, renal failure); wound interventions during study (debridement, surgery); Complications related to HBOT (seizure, pulmonary syndromes, vision disturbance; and all cause mortality
Time Frame
From enrollment up to 1 year after randomization
Title
Healthcare resource utilization: wound dressing materials; healthcare provider visits; inpatient hospital admissions; complex continuing care/rehabilitation; drug therapy; mobility assistive devices
Time Frame
From enrollment to study up to 1 year after randomization
Title
Quality of life: assessed by Standard Form 36 (SF-36) domain scores; EuroQoL 5D (EQ-5D) summary scores and by the Diabetic Foot Ulcer-Short Form (DFS-SF) scores
Time Frame
Baseline, end of treatment, end of follow-up, and EQ5D only at 6 and 12 months
Title
Cost effectiveness of HBOT: calculate the incremental cost per amputation avoided and the incremental cost per quality-adjusted life-year (QALY) gained
Time Frame
From Enrollment to 1 year after randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years Type 1 or 2 Diabetes Mellitus Wagner grading of foot lesions 3 or 4 on lower limb not healing for 4 weeks. Exclusion Criteria: Impending urgent amputation due to ongoing or exacerbated infection; Exposed calcaneus bone with no prospect of weight bearing potential even if defect has been healed; Dialysis-dependent renal failure; Any of the following medical conditions which preclude safe treatment in a monoplace chamber: clinical depression; severe dementia; claustrophobia; seizure disorder; active asthma; severe chronic obstructive pulmonary disease; previous thoracic surgery; previous spontaneous or trauma induced pneumothorax; history of severe congestive heart failure with left ventricular ejection fraction less than 20%; unstable angina; chronic sinusitis; chronic or acute otitis media or major ear drum trauma; severe kyphoscoliosis; arthritis; or morbid obesity; History of chemotherapy with use of Bleomycin; Participation in another investigative drug or device trial currently or within the last 30 days; Current candidates for vascular surgery, angioplasty or stenting; Major large vessel disease; Undergone vascular surgery or angioplasty within the last 3 months; Women who are currently pregnant or are breast feeding or women of childbearing potential who are not currently taking adequate birth control.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daria O'Reilly, PhD
Organizational Affiliation
Programs for Assessment of Technology in Health Research Institute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ludwik Fedorko, MD
Organizational Affiliation
Judy Dan Wound Care Centre/University Health Network
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ron Linden, MD
Organizational Affiliation
Judy Dan Wound Care Centre/University Health Network
Official's Role
Principal Investigator
Facility Information:
Facility Name
Judy Dan Wound Care Centre/University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M2R 1N5
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
21385365
Citation
O'Reilly D, Linden R, Fedorko L, Tarride JE, Jones WG, Bowen JM, Goeree R. A prospective, double-blind, randomized, controlled clinical trial comparing standard wound care with adjunctive hyperbaric oxygen therapy (HBOT) to standard wound care only for the treatment of chronic, non-healing ulcers of the lower limb in patients with diabetes mellitus: a study protocol. Trials. 2011 Mar 7;12:69. doi: 10.1186/1745-6215-12-69.
Results Reference
background
PubMed Identifier
26740639
Citation
Fedorko L, Bowen JM, Jones W, Oreopoulos G, Goeree R, Hopkins RB, O'Reilly DJ. Hyperbaric Oxygen Therapy Does Not Reduce Indications for Amputation in Patients With Diabetes With Nonhealing Ulcers of the Lower Limb: A Prospective, Double-Blind, Randomized Controlled Clinical Trial. Diabetes Care. 2016 Mar;39(3):392-9. doi: 10.2337/dc15-2001. Epub 2016 Jan 6.
Results Reference
derived

Learn more about this trial

Hyperbaric Oxygen Therapy (HBOT) for Chronic Diabetic Lower Limb Ulcers

We'll reach out to this number within 24 hrs