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Spots Global Cancer Trial Database for Morbidity Related to Secondary Hyperparathyroidism After Renal Transplantation

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Trial Identification

Brief Title: Morbidity Related to Secondary Hyperparathyroidism After Renal Transplantation

Official Title: Secondary Hyperparathyroidism Related Vascular and Bone Morbidity After Renal Transplantation - a 6 Year Follow up Retrospective Cohort Study.

Study ID: NCT01741064

Interventions

Study Description

Brief Summary: The purpose of the study is to evaluate the long term vascular morbidity and mortality in kidney transplant recipients based on one year post transplant levels of intact parathyroid hormone.

Detailed Description: Secondary hyperparathyroidism (SHPT) is a well known complication to chronic renal failure. With impaired renal function the phosphate excretion from the kidney is reduced. Together with low levels of 25- and 1,25-vitamin D3 and hypocalcemia this uremic mineral milieu drives the release of parathyroid hormone (PTH) and the development of SHPT. PTH has many functions but acts mainly to release calcium from the skeleton, to enhance calcium uptake from the intestines (by actions on vitamin D) and to lower serum phosphate by inducing phosphaturia. SHPT has been shown to cause vascular morbidity and fractures in the chronic kidney disease (CKD) patient. After successful renal transplantation (RT) the mineral disturbances are mostly recovered and stabilized at one year post RT, but in recent years it has been shown that SHPT persists in the major part of RT-recipients even after long term follow up. This has been associated with high risk of fractures and vascular related morbidity in the post transplant period. It has also been shown that low levels of iPTH in the post-transplant period might be associated with a high risk of fractures. Because of insufficient data on PTH levels and associated morbidity there is no specific recommendations of target PTH levels in the RT-patient. This indicates that there is need for further observational studies to describe the SHPT-associated morbidity in a post transplant cohort based on stabilized levels of post transplant iPTH.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Contact Details

Name: Gunnar Sterner, MD A/Prof

Affiliation: Dept of Nephrology and Transplantation Skane University Hospital Malmo

Role: STUDY_DIRECTOR

Name: Astrid Seeberger, PhD, A/Prof

Affiliation: ´Dept of nephrology, Karolinska University Hospital Huddinge, Stockholm

Role: STUDY_CHAIR

Name: Elin Isaksson, MD

Affiliation: Dept of Nephrology and Transplantation Skane University Hosptial Malmö

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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