A Study Comparing Outcomes of Kidney Transplants in Patients on Steroids Versus Those Who Discontinue Steroids
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ClinicalTrials.gov Identifier: NCT00273559 |
Recruitment Status : Unknown
Verified November 2007 by Florida Hospital Transplant Center.
Recruitment status was: Active, not recruiting
First Posted : January 9, 2006
Last Update Posted : May 12, 2008
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Condition or disease | Intervention/treatment |
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Kidney Diseases | Drug: prednisone |
The use of steroids after renal transplantation has been invaluable, resulting in higher rates of long term survival of the transplanted kidney. However, post-operative steroids are also associated with frequent post-operative and long term complications. There have been steroid elimination studies analyzing acute rejection rates, graft and patient survival. These studies show that many patients can safely have steroids withdrawn with equivalent results whan compared to those who remain on steroids.
With this study we will be using a rapid steroid elimination protocol for 40 patients and compare 20 patients who remain on steroids. We hope to show a decreased rate of complications such as osteopenia/osteoporosis, new onset diabetes, and a decrease in cardiovascular risk factors such as hyperlipidemia and hypertension.
Solumedrol will be given to all patients at the time of transplant followed by a prednisone taper. Those remaining on steroids will be discharged on prednisone 5 mg daily. Those in whom steroids are eliminated will be off prednisone by discharge.
Study Type : | Observational |
Estimated Enrollment : | 60 participants |
Observational Model: | Case-Control |
Time Perspective: | Prospective |
Official Title: | A Single Center, Open Label, Comparative, Controlled Trial to Assess the Risks and Benefits of Steroid Elimination vs. Steroid Therapy After Renal Transplantation |
Study Start Date : | January 2006 |
Estimated Study Completion Date : | December 2008 |

Group/Cohort | Intervention/treatment |
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1
subjects who remain on steroids after discharge
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2
Subjects will be off steroids at the time of discharge
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Drug: prednisone
group 2 will remain on 5 mg of prednisone for at least 90 days post transplant. |
- Acute rejection [ Time Frame: 6 months ]
- Patient and graft survival [ Time Frame: 6 months ]
- Incidence of infection [ Time Frame: one year ]
- Quality of life (health survey) [ Time Frame: one year ]
- Incidence of post-transplant diabetes [ Time Frame: one year ]
- Incidence of osteopenia/osteoporosis at baseline and one year [ Time Frame: one year ]
- Renal function [ Time Frame: one year ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Patients undergoing a single renal transplant from deceased or living donor
- Adults 18 years and older
- First or second renal transplant
- Capable of understanding the purposes of the study, has given written informed consent, and agrees to comply with the study requirements
- Women of child bearing age should have a negative serum pregnancy test
Exclusion Criteria:
- Greater than 2 renal transplants
- Age < 18 years
- Patients receiving immunosuppressive therapy within the preceding 28 days for first transplant and 3 months for the second transplant
- Cold ischemia time > 30 hours
- History of malignancy in the last 5 years except successfully treated localized non-melanoma skin cancer
- HIV, hepatitis B virus (HBV), or hepatitis C virus (HCV) positive serology
- Loss of previous transplant in < 1 year
- History of non-compliance
- Any form of substance abuse, psychiatric disorder or condition which, in the opinion of the investigator, may impair communication with the investigator or compliance with study procedures
- Multiple organ transplant
- History of chronic steroid use except for inhaled steroids for asthma
- Pregnant or lactating females
- Women of childbearing potential not willing to use a reliable form of contraception.
- Patients with severe medical condition(s) that, in the view of the investigator, prohibits participation in the study
- Known sensitivity to study drugs or class of study drugs
- Use of any investigational agent in the last 30 days

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00273559
United States, Florida | |
Florida Hospital Transplant Center | |
Orlando, Florida, United States, 32804 |
Principal Investigator: | Michael Angelis, MD | Florida Hospital Transplant Center |
Responsible Party: | Michael Angelis, MD, Florida Hospital Transplant Center |
ClinicalTrials.gov Identifier: | NCT00273559 |
Other Study ID Numbers: |
TL092005-1 |
First Posted: | January 9, 2006 Key Record Dates |
Last Update Posted: | May 12, 2008 |
Last Verified: | November 2007 |
Renal Transplantation |
Kidney Diseases Urologic Diseases Prednisone Anti-Inflammatory Agents Glucocorticoids |
Hormones Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Antineoplastic Agents, Hormonal Antineoplastic Agents |