Clinical Trials Directory

Trials / Unknown

UnknownNCT01316068

Effect of Sulodexide on Albuminuria in Chinese Type 2 Diabetic Patients

Effect of Intravenous and Oral Therapy With Sulodexide on Albuminuria in Type 2 Diabetic Patients

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Current therapies targeting albuminuria in diabetic nephropathy leave residual urinary albumin secretion, which meanwhile leave residual cardiovascular risk. Previous studies demonstrated that sulodexide could reduce albuminuria in type 2 diabetic patients. But no data concerning Chinese population is available. The investigators aim to provide evidence of effects of sulodexide on diabetic nephropathy in Chinese diabetic patients. Further the investigators also test the hypothesis that sequential administration of intravenous and oral replacement of the drug would gain an earlier and greater reduction of albuminuria, compared with oral use only.

Conditions

Interventions

TypeNameDescription
DRUGintravenous use of sulodexide followed by oral usePatients will be given sulodexide 1200 LSU per day intravenously for 2 weeks,then receive 1000 LSU per day orally for 50 weeks.
DRUGuse of sulodexide orally onlyPatients receive 1000 LSU per day orally for 52 weeks

Timeline

Start date
2011-03-01
Primary completion
2012-08-01
Completion
2012-08-01
First posted
2011-03-16
Last updated
2011-03-16

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT01316068. Inclusion in this directory is not an endorsement.