Trials / Completed
CompletedNCT00745589
Sevelamer Hydrochloride in Peritoneal Dialysis Patients
Use of Sevelamer Hydrochloride to Control Hyperphosphatemia and Reduce Calcification Burden in the Poor Peritoneal Dialysis Patients
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- The University of Hong Kong · Academic / Other
- Sex
- All
- Age
- 25 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
To test the hypothesis that second-line fixed low-dose sevelamer hydrochloride therapy is as effective as first-line high-dose sevelamer hydrochloride therapy in limiting the progression of cardiovascular calcification.
Detailed description
Cardiovascular disease accounts for nearly 50% of the mortality and is the most frequent cause of hospitalization in ESRD patients. Hyperphosphatemia is increasingly recognized to be an important predictor of mortality and cardiovascular death in ESRD patients and is largely attributed to the increased prevalence of vascular calcification.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | sevelamer hydrochloride | First-line higher dose (that is, 800mg TDS and up to a maximum of 1200mg TDS) sevelamer hydrochloride will be compared against low dose second-line sevelamer hydrochloride (that is, fixed dose of 400mg TDS) |
Timeline
- Start date
- 2008-07-01
- Primary completion
- 2014-10-01
- Completion
- 2015-01-01
- First posted
- 2008-09-03
- Last updated
- 2020-06-18
Locations
1 site across 1 country: Hong Kong
Source: ClinicalTrials.gov record NCT00745589. Inclusion in this directory is not an endorsement.