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The clinical study of hydrotalcite reducing serum phosphorus in maintained hemodialysis patients

The clinical study of hydrotalcite reducing serum phosphorus in maintained hemodialysis patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16007785
Enrollment
Unknown
Registered
2016-01-17
Start date
2016-01-25
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Chronic Kidney Disease(CKD 5D)

Interventions

experimental group:hydrotalcite
Control group:aluminium hydroxide

Sponsors

Xiamen Zhongshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patient who were maintained hemodialysis over 3 months; 2. aged between 18-80 years old; 3. male or female; 4. serum phosphorus >1.78mmol/L; 5. Didn't given any treatment of reducing phosphorus, including aluminium hydroxide, hydrotalcite and lanthanum carbonate; 6. Signed a letter of authorization for patients, allowing the use and disclosure of personal health information (or informed consent, if applicable).

Exclusion criteria

Exclusion criteria: 1. Patients of maintain hemodialysis less than 3 months; 2. Age less than 18 and over 80 years old; 3. Serum phosphorus <1.78mmol/L; 4. Have given any treatment of reducing phosphorus in 3 months, including aluminium hydroxide,hydrotalcite and lanthanum carbonate; 5. The patients whose refuse taking part in the trial; 6. Patients combined with tumour, active bleeding, infection and other acute inflammation; 7. Patients who maybe renal transplant or peritoneal dialysis or go to other hospital in half year; 8. Patients who die during trial.

Design outcomes

Primary

MeasureTime frame
serum phosphorum;Serum aluminium;

Secondary

MeasureTime frame
serum calcium;Serum parathyroid hormone ;

Countries

China

Contacts

Public ContactGuan Tianjun
guantianjun@aliyun.com+86 13950199068

Outcome results

None listed

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