Adjunctive Hyperbaric Oxygen Therapy (HBOT) for Lower Extermity Diabetic Ulcer:
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| ClinicalTrials.gov Identifier: NCT03675269 |
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Recruitment Status :
Withdrawn
(Study was moved to another location with involvement of different researchers)
First Posted : September 18, 2018
Last Update Posted : February 28, 2019
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Diabetic foot ulcers are associated with high risk of amputation. About 50% of patients undergoing non-traumatic lower limb amputations are diabetics5. The 5-year amputation rate is estimated to be 19% with a mean time to amputation 58 months since the onset of an diabetic foot ulcer6.Because infection and tissue hypoxia are the major contributing factors for non-healing diabetic foot ulcers, hyperbaric oxygen therapy (HBO) carries a potential benefit for treating these problematic wounds that do not respond to standard therapy.
The role of oxygen in the wound healing cascade and subsequent combatting action against bacterial invasion, especially anaerobes, is well documented.14 Delayed or arrested healing and the development of infection is a direct result from decreased perfusion and poor oxygenation of tissue.15 The presence of wound hypoxia is an major etiological pathway in the development of chronic non-healing diabetic foot ulcers
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Ulcer Foot Diabetic Foot Ulcer | Other: HBOT Behavioral: Standard wound care | Not Applicable |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 0 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Care Provider) |
| Primary Purpose: | Treatment |
| Official Title: | Adjunctive Hyperbaric Oxygen Therapy (HBOT) for Lower Extermity Diabetic Ulcer: A Prospective Double-Blind, Randomized Control Clinical Trail |
| Actual Study Start Date : | September 5, 2018 |
| Estimated Primary Completion Date : | September 2019 |
| Estimated Study Completion Date : | September 2019 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Treatment
HBOT
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Other: HBOT
Standard practice Behavioral: Standard wound care Standard wound care |
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Active Comparator: Control
Standard wound care
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Behavioral: Standard wound care
Standard wound care |
- Change in wound size [ Time Frame: 4 years ]The change of wound size at 4 weeks (granulation formation) as measured by the Silhouette three dimensional photography
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Any gender aged > 18 years.
- Confirmed type 1 or type 2 Diabetes Mellitus patient, currently on anti-diabetic medication
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Participant is to have at least one wound, which meets ALL of the following criteria: a. The ulcer to be present on the lower extremity below the ankle joint to make this study comparable to others done on diabetic patients b. Documented proof of chronicity (present for more than 3 months, despite conventional wound care).
c. Wagner classification Grade 3 or higher as recommended by the Undersea and Hyperbaric Medical Society.
- Meeting the selection for HBO criteria as determined by transcutaneous oxygen measurements.
- Willing and able to provide an informed consent for the study and related procedures.
Exclusion Criteria:
- Lower extremity or foot ulcers of non-diabetic peripheral vascular disease, venous, lymphedematous or neoplastic etiology.
- Having any condition or previous treatment that is known to be a contra-indicated for hyperbaric oxygen therapy.
- Pregnant or lactating females.
- Candidate with proven macro-vascular compromise who is not eligible for vascular intervention surgery.
- Previous treatment with hyperbaric oxygen therapy.
| Responsible Party: | King Hamad University Hospital, Bahrain |
| ClinicalTrials.gov Identifier: | NCT03675269 |
| Other Study ID Numbers: |
KingHamadUHBahrain |
| First Posted: | September 18, 2018 Key Record Dates |
| Last Update Posted: | February 28, 2019 |
| Last Verified: | February 2019 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Diabetic Foot Foot Ulcer Ulcer Pathologic Processes Diabetic Angiopathies Vascular Diseases Cardiovascular Diseases Leg Ulcer |
Skin Ulcer Skin Diseases Diabetes Complications Diabetes Mellitus Endocrine System Diseases Diabetic Neuropathies Foot Diseases |

