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A single-center prospective study of the effect of intravenous paricalcitol on anemia and inflammation for hemodialysis patients with secondary hyperparathyroidism

A single-center prospective study of the effect of intravenous paricalcitol on anemia and inflammation for hemodialysis patients with secondary hyperparathyroidism

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000032353
Enrollment
Unknown
Registered
2020-04-26
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Secondary Hyperparathyroidism, SHPT

Interventions

Case series:Paricalcitol

Sponsors

The First Affiliated Hospital of Shenzhen University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Ckd5d patients who received maintenance dialysis for at least 3 months, 3 times a week, single kt / V > 1.2; 2. First treatment patients: never received VitD and similar treatment; 3. Treated patients: they are being treated with VitD and its analogues, and PTH level is continuously higher than 300pg / ml, or it has a continuous upward trend in the past three tests; 4. Patients older than 18 years old; 5. Patients with baseline blood calcium less than 10.0 mg / dl (2.5 mmol / L).

Exclusion criteria

Exclusion criteria: 1. Patients whose serum level of iPTH was more than 1500pg / ml in the last two consecutive tests; 2. Allergic reaction to VD and its analogues; 3. Patients who received parathyroidectomy within one year; 4. Patients with indications for parathyroidectomy: (1) Patients with severe SHPT were resistant to active VD and its analogues; (2) Persistent hypercalcemia and / or hyperphosphatemia with ineffective drug treatment; (3) There is imaging evidence of at least one hyperparathyroidism. For example, high frequency color ultrasound shows that the diameter of the hyperparathyroidism is larger than 1cm and there is abundant blood flow; 5. Patients with severe infection; 6. Patients with malignant tumor; 7. Patients with a history of alcohol or drug abuse in the past 6 months; 8. Pregnant patients; 9. Patients with severe liver disease or liver dysfunction; 10. Patients who are allergic to or intolerable to any therapeutic drug; 11. Patients who were still participating in clinical studies of other drugs / devices 4 weeks before enrollment; 12. The researchers think that patients are not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Hb;iPTH;Ca;P;CRP;IL-1;IL-6;IL-8;IL-10;TNF-alpha;IFN-gama;AP;

Secondary

MeasureTime frame
Heart valve calcification score;Diameter of parathyroid gland;

Countries

China

Contacts

Public ContactQijun Wan

The First Affiliated Hospital of Shenzhen University

yiyuan2224@sina.com+86 13537857368

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026