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OpenTrials
Completed

NCT Number: NCT04967469

Comparison of Serum Calcium Level Between Preoperative Vitamin D and Non-vitamin D Regimen of Total Parathyroidectomy in End-stage Renal Failure Patients in Rajavithi Hospital

This Research is compare about IV Calcium between end-stage renal failure patients who take vitamin D and non-vitamin D preoperative parathyroidectomy

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • New End-stage renal failure patients and have iPTH>800 pg/dl at least 6 months
  • Patients who no response hyperphosphatemia with high dose vitamin D

Exclusion criteria

  • Allergy vitamin D
  • Pregnancy
  • Patients who parathyroidectomy have less than 4 gland

Treatment and study plan

calcitriol

Drug

end-stage renal failure patients who is hyperparathyroid with ESRD take calcidol preoperative Parathyroidectomy

Alfacalcidol 0.5 MCG Oral Capsule

Drug

end-stage renal failure patients who is hyperparathyroid with ESRD take alfacalcidol preoperative Parathyroidectomy

Primary outcomes

  1. Comparison of serum calcium level between patients who take Vitamin D and non-Vitamin D

    Time frame: 4 year

    Comparison of serum calcium level between patients who take Vitamin D and non-Vitamin D

Sponsors and collaborators

Lead sponsor

Department of Medical Services Ministry of Public Health of Thailand

Other Gov

Registry information

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Jul 19, 2021
Registry last updated
Jan 25, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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