Diabetic Foot Clinical Trial
Official title:
Randomized Study Comparing Different Durations of Antibiotic Treatment for Diabetic Foot Infections
Verified date | June 2020 |
Source | University Hospital, Geneva |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a randomized, unblinded, single-centre study. After eventual surgical debridement
(not amputation), patients will be randomized to receive 1 of 2 targeted antibiotic regimens,
in the ratio 1:1.
For diabetic toe osteomyelitis, the patients will be randomized between a 3 and a 6 week's
arm, for soft tissue infections between 10 and 20 days. The final assessments used in the
primary efficacy analysis will be obtained at the test-of-cure (TOC) visit approximately 60
days after treatment is stopped.
Status | Completed |
Enrollment | 182 |
Est. completion date | March 31, 2020 |
Est. primary completion date | February 29, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 120 Years |
Eligibility |
Inclusion Criteria: 1. Age = 18 2. Diabetes mellitus 3. Diabetic Foot Infections 4. Surgical intervention to remove all necrotic tissue or tenotomy. 5. Osteomyelitis limited to bone contact or cortical lesions in X-ray. Exclusion Criteria: 1. Implanted device. 2. More than 96 hours of systemic antibiotic therapy prior to inclusion 3. Amputation 4. Destructive osteomyelitis 5. Concomitant infections requiring more than 14 days of antibiotic therapy. |
Country | Name | City | State |
---|---|---|---|
Switzerland | Geneva University Hospitals | Geneva |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Geneva |
Switzerland,
Tone A, Nguyen S, Devemy F, Topolinski H, Valette M, Cazaubiel M, Fayard A, Beltrand É, Lemaire C, Senneville É. Six-week versus twelve-week antibiotic therapy for nonsurgically treated diabetic foot osteomyelitis: a multicenter open-label controlled rand — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Participants Experiencing Clinical Failure | Visual and dichotomous evaluation regarding the numbers of clinical recurrence/failure | 30-60 days | |
Secondary | Number of Participants Experiencing Adverse Events Related to the Antibiotic Therapy | Adverse events related to the antibiotic therapy. | 30-60 days |
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