Trials / Completed
CompletedNCT01970605
Silver Graft All Comers Registry
Silver Graft All Comers Registry is to Assess the Long Term Clinical Benefit of Silver Graft in an Unselected Patient Population
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 230 (actual)
- Sponsor
- B. Braun Melsungen AG · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
This web based e-Registry will be international, multi-center and prospective. Silver Graft e-Registry to assess the long term clinical benefit of Silver Graft in an unselected patient population
Detailed description
To assess the long term clinical benefit of Silver Graft in an unselected patient population with Peripheral Artery Occlusive Disease (PAOD) fulfilling one of the the following criteria: 1. Any suitable patient in need of an infrarenal vascular reconstruction with Fontaine class IIb or indicated vascular reconstruction aneurysm repair. or 2. Any suitable patient with an increased risk for early graft failure except those mentioned under (3). These may include * diabetics * Fontaine class\> IIb * patients of advanced age (≥75 y) * patients with renal insufficiency (creatinine ≥ 1.50 mg/dl or ≥130 µmol/l) * patients with COPD or documented coronary artery disease (prior PCI, prior CABG, documented myocardial ischemia) * patients with major amputation * immunosuppressed patients * patients with autoimmune disease, malignancy or 3. Any suitable patient with graft infection or present infection in the anatomical position of indicated vascular reconstruction.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Surgical reconstruction | In contrast to silver acetate impregnated vascular graft, Silver Graft can be immersed in an antibiotic containing solution prior to implantation. This practice should always be followed according to each participant's hospital guidelines and experience. The long term efficacy of the metallic silver coating will not be reduced. Common practice antibiotic co-medication before, during and after surgery needs to be documented but is at the discretion of each participating institution. Due to the registry character of this assessment, i.e. routine use of the investigational product, local antibiotics, e.g. dipping of the vascular graft into a rifampin solution is permissible. |
Timeline
- Start date
- 2013-10-01
- Primary completion
- 2017-12-01
- Completion
- 2018-12-01
- First posted
- 2013-10-28
- Last updated
- 2019-01-23
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01970605. Inclusion in this directory is not an endorsement.