3M, Diabetes and Endocrine Research Center
Hong Kong
Location status: Recruiting
Location contact
Elaine Chow, MD
CONTACT
Elaine Chow, MD
PRINCIPAL_INVESTIGATOR
Shun Ling KONG, MN
CONTACT
NCT Number: NCT06727409
To evaluate triple therapy with nsMRA, RASi and SGLT2i on albuminuria in individuals with T2D and CKD
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 4
Hong Kong
Location status: Recruiting
Elaine Chow, MD
CONTACT
Elaine Chow, MD
PRINCIPAL_INVESTIGATOR
Shun Ling KONG, MN
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Finerenone 10mg or 20 mg as tolerated on top of maximal tolerated RASi and stable SGLT2i therapy
Time frame: 26 weeks
urine ACR between baseline and end of study (26 weeks)
Time frame: 26 weeks
eGFR calculated from plasma creatinine from baseline to end of study in ml/min/1.73m2
Time frame: 26 weeks
Change in plasma potassium (mmol/l) from baseline to end of study
Time frame: 26 weeks
Change in systolic and diastolic blood pressure (mmHg) from baseline to end of study
Time frame: 26 weeks
change in HRQoL from baseline to end of study using EQ5D
Time frame: 26 weeks
Change in body weight (kg) from baseline to end of study
Contact information is provided by the study sponsor or research team.
Chinese University of Hong Kong
Other
Acronym: RAiSiN
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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