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Decline in COVID cases
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This will be a randomized trial of maintenance versus reduction in immunosuppression in adult patients (age >18 years old) with functioning renal transplants admitted to hospital with confirmed COVID-19 disease.
The optimal management of immunosuppression in renal transplant patients with COVID-19 disease is unclear. On one hand, many centers advocate reduction of immunosuppression in infected patients, with the rationale that such an approach will unleash the anti-viral T-cell response. However, on the other hand, some centers advocate there may be rationale to maintain baseline immunosuppression in order to mitigate against development of an uncontrolled over-activation of the immune response. The investigators propose to address this knowledge gap by performing a randomized clinical trial that will test formal comparisons of maintenance versus reduction in immunosuppression.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Maintenance of Immunosuppression | Experimental | Maintenance of immunosuppression (defined as no change to pre-admission immunosuppression, or reduction in anti-metabolite by up to 50% (to a minimum of MMF 500 mg per day or azathioprine 50 mg per day) |
|
| Reduction of Immunosuppression | Active Comparator | Reduction of immunosuppression (defined as anti-metabolite withdrawal plus reduction of tacrolimus or cyclosporin, to a minimum target trough concentration of 3 ng/mL for tacrolimus and 50 ng/mL for cyclosporin). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Maintenance or reduction of immunosuppression | Other | Maintenance versus reduction of immunosuppression |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in IL-6 concentration from baseline to day 7 | baseline to day 7 |
| Measure | Description | Time Frame |
|---|---|---|
| Change in IL-6 concentration from baseline to day 28 | Baseline to day 28 | |
| Change in T cell response to SARS-CoV-2 | Baseline to day 7 and day 28 | |
| Change in titer of serum anti-SARS-CoV-2 antibodies |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jamil Azzi, MD, PhD | Birgham and Women's Hospital | Principal Investigator |
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Single-blind, parallel-group, randomized, active-controlled trial
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This is a single-blind trial, in that only the assessor will be blinded to the treatment assignment.
| Baseline to day 7 and day 28 |
| Change in COVID-19 disease severity score (range 1 to 8; higher worse) | Through day 28 |
| Proportion of patients needing non-invasive ventilation or intubation | Through day 28 |
| Proportion of patients developing ANC < 500 cells per microliter | Through day 28 |
| Proportion of patients developing lymphopenia < 400 cells per microliter | Through day 28 |
| Length of hospital stay | Through day 28 |
| Proportion of patients developing biopsy-proven acute rejection | Through day 28 |
| In-hospital and 28-day mortality | Through day 28 |
| Adverse and serious adverse events | Through day 28 |
| ID | Term |
|---|---|
| D008283 | Maintenance |
| ID | Term |
|---|---|
| D005159 | Health Care Facilities Workforce and Services |
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