Trials / Completed
CompletedNCT04081792
Optimal Antibiotics for Operated Diabetic Foot Infections
Optimization of the Surgical and Medical Management of Diabetic Foot Infections
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 643 (actual)
- Sponsor
- Balgrist University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 99 Years
- Healthy volunteers
- Not accepted
Summary
Diabetic foot problems, especially infections (DFI), require multiple resources including iterative surgeries and amputations, long-lasting antibiotic therapies, education, off-loading and eventually revascularization and appropriate foot-ware. Treatment is complicated, multidisciplinary, and marked with a high risk of recurrences. This is a retrospective and prospective cohort with side studies of pathologies and academic research questions that cannot be separated from each other. The investigators establish a retro-and prospective cohort of diabetic foot problems (ambulatory and hospitalized patients) and perform side studies to reduce the incidence of complications, and to reduce recurrences of DFI, cost and adverse events related to therapies. Cohort: Prospective and retrospective cohort of all diabetic foot problems with emphasis on surgical and infectious variables. Trial 1 (Randomized trial on residual infection after amputation): Determination of the level of amputation per MRI followed by a randomization concerning the duration of post-amputation systemic antibiotic therapy, if there is residual bone infection. Trial 2 (Randomized trial on infection without amputation): Determination of the duration of systemic antibiotic therapy in diabetic foot infections without Amputation of the infection.
Detailed description
Trial 1: At enrollment (Day 1), the investigator will prescribe empiric antibiotic treatment based on instructions provided in the protocol and determine the most appropriate route of administration (oral or IV) according to the patient's condition. Patients will be randomized in the ratio 1:1 between 1 versus 4 days for post-amputation soft tissue infections; and between 1 versus 3 weeks if there is microbiologically proven residual bone infection/contamination in the proximal stump samples of the residual bone. Trial 2: At enrollment (Day 1), the investigator will prescribe empiric antibiotic treatment based on instructions provided in the protocol and determine the most appropriate route of administration (oral or IV) according to the patient's condition. Patients will be randomized in the ratio 1:1 between 10 versus 20 days for post-debridement soft tissue infections; and between 3 versus 6 weeks for diabetic foot osteomyelitis post.-debridement (without amputation).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Antibiotic therapy | Postoperative randomizations regarding the duration of systemic antibiotics |
Timeline
- Start date
- 2019-09-04
- Primary completion
- 2024-12-31
- Completion
- 2025-03-01
- First posted
- 2019-09-09
- Last updated
- 2025-06-17
Locations
1 site across 1 country: Switzerland
Source: ClinicalTrials.gov record NCT04081792. Inclusion in this directory is not an endorsement.