A Prospective Cohort Study to Describe the Evolution of Persistent Hyperparathyroidism in Kidney Transplant Recipients

Sponsor
The Cleveland Clinic (Other)
Overall Status
Completed
CT.gov ID
NCT01163669
Collaborator
Amgen (Industry)
15
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28.1
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Study Details

Study Description

Brief Summary

The purpose of this study is to see if Hyperparathyroidism (HPT) is common in people who receive a kidney transplant. Patients with HPT often have high parathyroid hormone (PTH) levels and may have large parathyroid glands in the neck. Patients with HPT can develop bone disease (osteodystrophy). This bone disease can cause bone pain, fractures, and poor formation of red blood cells. Other problems from HPT may include increases in blood levels of calcium (hypercalcemia) and low blood levels of phosphorus (hypophosphatemia). The high calcium levels may cause calcium to deposit in body tissues. Calcium deposits can cause arthritis (joint pain and swelling), muscle inflammation, itching, gangrene (death of soft tissue), heart and lung problems, or kidney transplant dysfunction (worsening of kidney transplant function). The purpose of this research study is to better understand the evolution of Hpt in people during the first 12 months after receiving a kidney transplant.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Subjects are enrolled in the study and a 12-month observational phase will begin. During the observational phase, subjects will attend a total of 8 visits at approximately 1, 2, 4, and 8 weeks after kidney transplantation and at 3, 6, 9, and 12 months after kidney transplantation. During these visits, subjects will have a review of medication history, blood tests, and a kidney function test. The blood will be used to test the level of certain components of you blood to see if your HPT has resolved, stabilized, or advanced. At selected visits throughout the study, you will have a urine sample collected and a health questionnaire that will ask about your health. Information regarding transplant kidney biopsy (if performed) also will be collected.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    15 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    A Prospective Cohort Study to Describe the Evolution of Persistent Hyperparathyroidism in Kidney Transplant Recipients
    Study Start Date :
    Jul 1, 2010
    Actual Primary Completion Date :
    Nov 1, 2012
    Actual Study Completion Date :
    Nov 1, 2012

    Arms and Interventions

    Arm Intervention/Treatment
    kidney transplant recipients

    Outcome Measures

    Primary Outcome Measures

    1. plasma parathyroid hormone(PTH)level [12 months]

    Secondary Outcome Measures

    1. corrected total serum calcium and phosphorus concentration [12 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • diagnosis of CKD receiving hemodialysis prior to transplant;

    • admission for kidney transplant surgery;

    • men and women at least 18 year of age;

    • one or more plasma PTH values determined during during the 6 months before screening that is greater the 65pg/ml;

    • plasma PTH greater than 65pg/ml at screening before kidney transp[lant as measured by the central lab.

    Exclusion Criteria:
    • history of medical conditions that cause hypercalcemia such as primary HPT, active malignancy, and granulomatous diseases.

    • receipt of multiple organ transplant.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Cleveland Clinic Cleveland Ohio United States 44195

    Sponsors and Collaborators

    • The Cleveland Clinic
    • Amgen

    Investigators

    • Principal Investigator: T Srinivas, MD, MD, The Cleveland Clinic

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    The Cleveland Clinic
    ClinicalTrials.gov Identifier:
    NCT01163669
    Other Study ID Numbers:
    • 20080093
    First Posted:
    Jul 16, 2010
    Last Update Posted:
    Aug 13, 2013
    Last Verified:
    Jan 1, 2012
    Keywords provided by The Cleveland Clinic
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 13, 2013