Clinical Trials Directory

Trials / Terminated

TerminatedNCT03152084

The Study Will Evaluate Average 24-hr Sodium Excretion During Dapagliflozin Treatment in Patients With Type 2 Diabetes Mellitus With Preserved or Impaired Renal Function or Non-diabetics With Impaired Renal Function.

DAPASALT: An Open Label, Phase IV, Mechanistic, Three-Arm Study to Evaluate the Natriuretic Effect of 2-Week Dapagliflozin Treatment in Type 2 Diabetes Mellitus Patients With Either Preserved or Impaired Renal Function and Non-Diabetics With Impaired Renal Function

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
24 (actual)
Sponsor
AstraZeneca · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate how dapagliflozin mechanism of action is impacted by Type 2 Diabetes Mellitus status and kidney function

Conditions

Interventions

TypeNameDescription
DRUGDapagliflozinThe study consists of a 2-week, open label, dapagliflozin (10mg) treatment period.

Timeline

Start date
2017-07-12
Primary completion
2020-03-20
Completion
2020-03-20
First posted
2017-05-12
Last updated
2021-05-28
Results posted
2021-05-28

Locations

4 sites across 2 countries: Netherlands, Sweden

Source: ClinicalTrials.gov record NCT03152084. Inclusion in this directory is not an endorsement.

The Study Will Evaluate Average 24-hr Sodium Excretion During Dapagliflozin Treatment in Patients With Type 2 Diabetes M (NCT03152084) · Clinical Trials Directory