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Clinical Trial Summary

The aim of this study is to assess the clinical, laboratory and vascular calcification outcome within 6 months duration in patients undergoing surgical parathyroidectomy (total, subtotal, and total with autotransplantation)


Clinical Trial Description

All patients above the age of 18, with end stage renal disease maintained on regular hemodialysis and are indicated for surgical parathyroidectomy. The indications for parathyroidectomy included persistently elevated intact parathormone hormone levels of greater than 500 pg/mL, uncontrolled hypercalcaemia with hyperphosphataemia or clinical symptoms of secondary hyperparathyroidism refractory to medical treatment. These symptoms included bone pain, pruritus, fracture, fatigue and calciphylaxis These patients will be exposed to pre-operative evaluation of clinical, laboratory and vascular calcification in abdominal aorta and coronary calcium scoring using ECG- gated non contrast CT in hemodialysis patients undergoing parathyroidectomy Post-operative evaluation of clinical, laboratory and vascular calcification in abdominal aorta and coronary calcium scoring using non contrast CT will be done 6 months post-operative Assessment of the relation between preoperative and postoperative measures Patients with the following criteria will be excluded: 1. chronic kidney disease patients not yet on regular Hemodialysis 2. patients who had primary hyperparathyroidism 3. patients who had received kidney transplantation 4. patients who underwent repeated parathyroidectomy 5. patients who were lost to follow-up or with missing data. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03724188
Study type Observational
Source Mansoura General Hospital
Contact
Status Completed
Phase
Start date November 30, 2017
Completion date October 30, 2021