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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00745719
Other study ID # A111-102
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2007
Est. completion date January 2012

Study information

Verified date August 2020
Source The University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To test the hypothesis that total parathyroidectomy retards cardiovascular calcification, improves bone mineral density, reduces cardiac hypertrophy and arterial stiffening in end-stage renal disease patients on maintenance dialysis.


Description:

Secondary hyperparathyroidism (SHPT) in patients with end-stage renal disease contributes to increased cardiovascular morbidity and mortality via different mechanisms. Uncontrolled hyperparathyroidism is associated with left ventricular hypertrophy and has been implicated in the development of cardiac interstitial fibrosis and diastolic dysfunction.


Recruitment information / eligibility

Status Completed
Enrollment 122
Est. completion date January 2012
Est. primary completion date September 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Endstage renal disease patients receiving either long-term hemodialysis or peritoneal dialysis treatment, with elevated intact parathyroid hormone (iPTH) levels > 500pg/ml on two or more occasions.

- Patients with parathyroid nodular or diffuse hyperplasia identified by ultrasound imaging or radioisotope scan.

- Patients who provide informed consent for the study.

Exclusion Criteria:

- Patients with significant background valvular heart disease

- Patients who are unfit for general anaesthesia

- Patients with acute myocardial infarction within recent two months

- Patients with poor general condition

- Patients with plans for living related kidney transplant within 1 year

- Patients with previous history of parathyroidectomy

- Patients with calciphylaxis

- Patients with underlying active malignancy

- Patients with contraindication for MRI

Study Design


Intervention

Procedure:
parathyroidectomy
total parathyroidectomy with forearm autografting

Locations

Country Name City State
Hong Kong Queen Mary Hospital, Tung Wah Hospital Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
The University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in vascular and valvular calcium scores 12 months
Secondary Change in bone mineral density 12 months
Secondary change in aortic pulse wave velocity, 12 months
Secondary change in left ventricular mass, volume and function 12 months
Secondary changes in quality of life scores 12 months
Secondary changes in iPTH 6 and 12 months
Secondary changes in Serum calcium and phosphate 6 and 12 months
Secondary changes in alkaline phosphatase 6 and 12 months
Secondary changes in handgrip strength 12 months
Secondary changes in subjective global assessment 6 and 12 months
Secondary changes in serum albumin 6 and 12 months
Secondary changes in inflammatory marker 12 months
Secondary changes in HOMA index 6 and 12 months
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