Observational Study in Patients With Autosomal Dominant Polycystic Kidney Disease
| Status: | Completed |
|---|---|
| Conditions: | Renal Impairment / Chronic Kidney Disease |
| Therapuetic Areas: | Nephrology / Urology |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 2/4/2013 |
| Start Date: | June 2011 |
| End Date: | June 2014 |
| Contact: | OVERTURE Study Info |
| Email: | OVERTUREStudyInfo@mmgct.com |
A Multi-center, Longitudinal, Observational Study of Patients With Autosomal Dominant Polycystic Kidney Disease (ADPKD) to Establish the Rate, Characteristics, and Determinants of Disease Progression
To collect characteristics of patients with ADPKD across a broad population, over time to
better understand disease progression (signs, symptoms and outcomes). Association with
total kidney volume changes and other measures of disease progression will be determined in
order to identify a population at increased risk for disease progression. The economic and
quality life impact of ADPKD will be assessed. Subjects who terminated participation early
from clinical trials with tolvaptan may also be followed.
Inclusion Criteria:
- existing diagnosis of ADPKD by modified-Ravine criteria
- Total kidney volume >= 300 cc/m height by ultrasound or >= 250 cc/m height by MRI
Exclusion Criteria:
- Current or expected (within the next six months) interventions for the treatment of
ADPKD affecting kidney volume
We found this trial at
37
sites
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