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| ID | Type | Description | Link |
|---|---|---|---|
| 2009-014292-52 | EudraCT Number |
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The purpose of this study is to compare the effectiveness of tacrolimus (prograf) versus prednisolone for the treatment of nephrotic syndrome secondary to minimal change disease.
Minimal change disease is a common cause of nephrotic syndrome in adults. Standard treatment is with high dose steroids which is often effective in controlling the nephrotic syndrome but has a high morbidity due to the side effects of the steroids. There is also a high relapse rate,therefore many patients require long term steroid therapy to control their disease which has significant morbidity and mortality. Some patients are or also become steroid resistant. There are studies showing the effectiveness of alkylating agents such as cyclophosphamide but the use of these drugs is limited by their toxicity, including increased rates of infection, cancers and infertility.
Tacrolimus (prograf) is a T-cell specific calcineurin inhibitor that shares similar immunosuppressive actions with cyclosporine A.In other glomerular diseases such as focal segmental glomerulosclerosis and membranous glomerulonephritis, prograf has been shown to be a very effective treatment for proteinuria. This may be due to the immunomodulatory effects on the underlying disease, but there may also be a direct effect of tacrolimus (prograf) on the podocyte, stabilising the actin cytoskeleton and therefore decreasing protein leak.Therefore tacrolimus (prograf) is likely to be effective in reducing proteinuria in minimal change disease.It has also been shown to have a good side effect profile when used to allow the avoidance of steroids in transplantation.This study aims to prospectively study if tacrolimus (prograf) is effective as treatment for minimal change disease compared with standard therapy with steroids, and whether it has advantages in terms of side effect profile and prevention of relapse.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| prednisolone | Active Comparator | prednisolone tablets |
|
| tacrolimus | Experimental | tacrolimus tablets |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| tacrolimus | Drug | tacrolimus0.05mg/kg bd (levels 6-12ng/ml) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of Participants Achieving Complete Remission From Nephrotic Syndrome at 8 Weeks | normalisation of serum albumin and urine PCR <50 units | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of Patients Achieving Complete Remission From Nephrotic Syndrome at 16 and 26 Weeks | 16 and 26 weeks | |
| Percentage of Patients Achieving Remission Who Then Relapse | 2 years | |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Megan Griffith, MBChBPhDFRCP | Imperial College NHS Trust | Study Chair |
| Tom Cairns, MBBSMRCP | Imperial College NHS Trust | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hammersmith Hospital | London | W12 OHS | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 35230699 | Derived | Azukaitis K, Palmer SC, Strippoli GF, Hodson EM. Interventions for minimal change disease in adults with nephrotic syndrome. Cochrane Database Syst Rev. 2022 Mar 1;3(3):CD001537. doi: 10.1002/14651858.CD001537.pub5. |
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| ID | Title | Description |
|---|---|---|
| FG000 | Prednisolone | prednisolone tablets prednisolone: Prednisolone 1mg/kg maximum 60mg od |
| FG001 | Tacrolimus | tacrolimus tablets tacrolimus: tacrolimus0.05mg/kg bd (levels 6-12ng/ml) |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Prednisolone | prednisolone tablets prednisolone: Prednisolone 1mg/kg maximum 60mg od |
| BG001 | Tacrolimus | tacrolimus tablets tacrolimus: tacrolimus0.05mg/kg bd (levels 6-12ng/ml) |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Customized | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Percentage of Participants Achieving Complete Remission From Nephrotic Syndrome at 8 Weeks | normalisation of serum albumin and urine PCR <50 units | Patients at 8 weeks of therapy- on intention to treat basis | Posted | Count of Participants | Participants | 8 weeks |
|
Up to 3 years
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Prednisolone | prednisolone tablets prednisolone: Prednisolone 1mg/kg maximum 60mg od |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| diverticualr disease | Gastrointestinal disorders | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| various non serious | General disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Dr Megan Griffith | Imperial College NHS Trust | 02033137309 | m.e.griffith@imperial.ac.uk |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Feb 2, 2013 | Mar 16, 2021 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D009402 | Nephrosis, Lipoid |
| ID | Term |
|---|---|
| D009401 | Nephrosis |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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| ID | Term |
|---|---|
| D016559 | Tacrolimus |
| D011239 | Prednisolone |
| ID | Term |
|---|---|
| D018942 | Macrolides |
| D007783 | Lactones |
| D009930 | Organic Chemicals |
| D011246 | Pregnadienetriols |
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| prednisolone | Drug | Prednisolone 1mg/kg maximum 60mg od |
|
| Number of Serious Adverse Events |
| 3 years |
| Change in Baseline Glomerular Filtration Rate | 3 years |
| BG002 | Total | Total of all reporting groups |
| Participants |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race and Ethnicity Not Collected | Race and Ethnicity were not collected from any participant. | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Units | Counts |
|---|---|
| Participants |
|
|
|
| Secondary | Percentage of Patients Achieving Complete Remission From Nephrotic Syndrome at 16 and 26 Weeks | Patients on intention to treat basis | Posted | Count of Participants | Participants | 16 and 26 weeks |
|
|
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| Secondary | Percentage of Patients Achieving Remission Who Then Relapse | Posted | Count of Participants | Participants | 2 years |
|
|
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| Secondary | Number of Serious Adverse Events | Posted | Number | serious adverse events | 3 years |
|
|
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| Secondary | Change in Baseline Glomerular Filtration Rate | data not collected | Posted | 3 years |
|
|
| 0 |
| 25 |
| 4 |
| 25 |
| 18 |
| 25 |
| EG001 | Tacrolimus | tacrolimus tablets tacrolimus: tacrolimus0.05mg/kg bd (levels 6-12ng/ml) | 0 | 27 | 3 | 27 | 20 | 27 |
| headache | Nervous system disorders | Systematic Assessment |
|
| fracture radius | Musculoskeletal and connective tissue disorders | Systematic Assessment |
|
| respiratory infection | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
|
| hypertension | Cardiac disorders | Systematic Assessment |
|
| rash and diarhoaea | Skin and subcutaneous tissue disorders | Systematic Assessment |
|
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| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D011245 |
| Pregnadienes |
| D011278 | Pregnanes |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |