Steroid Withdrawal Immunosuppression After Renal Transplantation

NCT ID: NCT01550445

Last Updated: 2012-03-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-05-31

Study Completion Date

2012-07-31

Brief Summary

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The investigators analyze the clinical outcome of steroid withdrawal protocol starting at 3 months after kidney transplantation using tacrolimus, Mycophenolate Mofetil (MMF), and basiliximab. This study is an open-label, prospective, controlled clinical trial in a single center. Those patients who fulfill the entry criteria could enter in this prospective controlled trial of steroid withdrawal three months after transplantation.

Detailed Description

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Those patients who fulfill the entry criteria enter in this prospective controlled trial of steroid withdrawal starting at three months after transplantation. The entry criteria include 1) no episode of clinically treated nor biopsy confirmed acute rejection up to entry; 2) serum creatinine level equal to or less than 2 mg/mL on three separate measurements; 3) no proteinuria (urine protein less than 1000 mg/24 hours; 4) tacrolimus trough level \> 5 ng/ml without signs of nephrotoxicity; 5) agreement to follow the study protocol.

For the patients who enter into the protocol, prednisolone would be slowly withdrawn by 2.5 mg in every two weeks until 8 weeks after entering the protocol (5 months post-transplantation). The patients visit every week, and they are closely monitored with symptoms and signs, blood cell count, chemistry, and urinalysis.

Conditions

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Disorder Related to Renal Transplantation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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steroid withdrawal

The clinical outcome after kidney transplantation, under the immunosuppression of steroid withdrawal starting at 3 months post-transplantation using tacrolimus, mycophenolate mofetil, and basilixumab should be analyzed.

Group Type NO_INTERVENTION

Prednisolone

Intervention Type DRUG

Those patients who fulfill the entry criteria enter in this prospective controlled trial of steroid withdrawal starting at three months after transplantation

Interventions

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Prednisolone

Those patients who fulfill the entry criteria enter in this prospective controlled trial of steroid withdrawal starting at three months after transplantation

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients aged more than 13 years who received a primary kidney transplant
* Subject who is using CNI ± purine synthesis inhibitor + steroid without change within the past 3 months (except the dosage)
* serum creatinine \< 2 mg/dL and the variation of serum creatinine \< 30% during the past 3 months
* Proteinuria ≤ 1g quantified by 24 hour urine or spot urine protein/creatinine ratio \< 1.0
* Subjects who agree with written informed consent

Exclusion Criteria

* Subjects who received combined non-renal transplantation.
* Subject who received re-transplantation
* Deceased donor without a heartbeat
* Patients with hypersensitivity to Mycophenolate sodium, Mycophenolate acid or Mycophenolate Mofetil or to any of the excipients.
* Patient with HGPRT(Hypoxanthin e-guanine phosphoribosyl-transferase) such as Lesch-Nyhan syndrome and kelley-Seegmiller syndrome.
* HLA-identical living related donor
* ABO blood group incompatible
* HIV, HBsAg, or HCV Ab tests (+)
* Abnormal liver function test (AST or ALT or total bilirubin\> upper normal limit x3) ANC \< 1,500/μL or WBC \< 2,500/μL or platelet \< 750,000/μL
* Women who are either pregnant, lactating, planning to become pregnant in the next 12 months.
* Subjects with history of cancer, except successfully treated, localized nonmelanocytic skin cancer Subjects with clinically significant infections within the past 3 months.
Minimum Eligible Age

13 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ajou University School of Medicine

OTHER

Sponsor Role lead

Responsible Party

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Chang kwon oh

Professor, Department of Surgery

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Chang kwon oh, M.D.,Ph. D.

Role: PRINCIPAL_INVESTIGATOR

Department of surgery, Ajou University School of Medicine

Locations

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Ajou University Hospital

Suwon, , South Korea

Site Status RECRUITING

Countries

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South Korea

Central Contacts

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chang-kwon Oh, M.D

Role: CONTACT

82-10-9165-7281

Facility Contacts

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chang-kwon oh, M.D.

Role: primary

82-10-91657281

References

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Oh CK, Kim SJ, Kim JH, Lee JH. Prospective controlled protocol for three months steroid withdrawal with tacrolimus, basiliximab, and mycophenolate mofetil in renal transplant recipients. J Korean Med Sci. 2012 Apr;27(4):337-42. doi: 10.3346/jkms.2012.27.4.337. Epub 2012 Mar 21.

Reference Type DERIVED
PMID: 22468094 (View on PubMed)

Other Identifiers

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AJIRB-CRO-08-067

Identifier Type: -

Identifier Source: org_study_id

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