Ongoing Clinical Trials
BaxPA trial: A study to assess efficacy and safety of Baxdrostat in Adults with Primary Aldosteronism
This study will research a new medication to treat Primary Aldosteronism. This medication works to decrease the production of aldosterone.
This study will last for approximately 1 year. Participants will receive a placebo or the study medication for the first 8 weeks of the study. Then, everyone will receive the study medication up to week 44. Finally, participants will receive placebo or study medication for the final 8 weeks of the study.
The study will look at whether blood pressure control gets better. It will also assess changes in electrolytes, such as potassium and sodium and will measure if other lab tests change. Adults living with primary aldosteronism will be included. They should expect to be on stable blood pressure medication. Some of these medications may need adjusting by the study doctor at the beginning of this study. There are a total of 14 study visits, occurring every 2 weeks until week 16, and every 4-10 weeks afterwards until week 54.
Participants will be followed very closely by the study team to manage the symptoms of primary aldosteronism and any changes to health as a result of participating in this study.
Eligible ages: 18 to 100
Inclusion criteria:
1) Male of female ≥ 18 years old
2) Diagnosed with Primary Aldosteronism
3) Are willing to stop some medications that treat blood pressure, as directed by the study doctor (Mineralcorticoid Receptor Antagonists and potassium-sparing diuretics)
4) Must have healthy kidney functions as indicated by eGFR > 45 at screening visit
5) Specific serum potassium levels at screening
6) Females of child-bearing-potential must be willing to use contraception up to one month after the study medication has been stopped
Exclusion criteria:
1) Excessively high or low blood pressure
2) Surgical treatment for kidney issues must be evaluated
3) Other heart, liver, endocrine or secondary causes of hypertension considered relevant in the protocol or by the study doctor
4) Current medications will be reviewed and assessed by the study team and may be exclusionary or require adjustment
For more information, contact study coordinator Michelle Smith
mahunter@ucalgary.ca
403-955-8117
ZONE trial: Effect of ZT-01 On Nocturnal hypoglycemia Events in type 1 diabetes mellitus
We are looking for people living with type 1 diabetes who have ongoing low blood sugar, particularly at night, but have otherwise stable diabetes management. Participants should not have frequent severe hypoglycemia or recent visits to the hospital because of diabetes problems.
This study will explore if a new medication, only available in a research study, can reduce nighttime low blood sugar events.
One of three drug doses will be compared to a placebo for each research participant to see if blood sugars are better managed overnight and throughout the day.
Total time in study is approximately 18 weeks (4.5 months). Study visits are conducted in the mornings at the Clinical Trials Unit at Richmond Road Diagnostic and Treatment Centre.
Eligible ages: 18 to 75
Inclusion criteria:
1) Adult living with Type 1 Diabetes for at least 5 years
2) Nighttime low blood sugar is a recurring issue (<3.0mmol/L bimonthly, or time-below-range ≥1% in an ambulatory glucose profile average over 28 days)
3) Stable diabetes management routine (diet and exercise, medications)
4) Not planning a pregnancy and agree to use highly effective birth control
5) Other clinically relevant markers of health must be reviewed by the investigator
Exclusion criteria:
1) Hospitalization for Diabetic Ketoacidosis in the last 6 months will be reviewed
2) Severe hypoglycemia requiring assistance in the last 3 months will be reviewed
For more information, contact study coordinator Michelle Smith
mahunter@ucalgary.ca
403-955-8117
Cardiovascular Outcomes Trial
CLOSED for enrollment
SYNCHRONIZE CVOT STUDY
Investigative Incretin -3.6mg/6.0mg/placebo
High Risk for CVD, or have CKD
with or without Type 2 Diabetes
SUGARNSALT Trial
Effectiveness and safety of sotagliflozin in slowing kidney function decline in persons with type 1 diabetes and moderate to severe diabetic kidney disease: The SUGARNSALT Trial
The purpose of this study is to find out if a drug called sotagliflozin (SOTA) can slow kidney function decline in persons with type 1 diabetes and moderate to severe diabetic kidney disease (defined as greater than 50% reduction in kidney filtering function and the leakage of increased amounts of protein in the urine).
The study will enroll 150 participants and last 3.5 years. Participants will have:
- Type 1 Diabetes with moderate kidney dysfunction
- Must be willing to monitor blood glucose and ketones throughout the study
For more information contact:
Jenny Schulz
Email: jennifer.schulz@ucalgary.ca
Phone: (403)-955-8119
Eli Lilly - Incretin Study
AN INVITATION TO THE
TRANSCEND-T2D-2 CLINICAL STUDY
Retatrutide vs Semaglutide
Type 2 Diabetes
mahunter@ucalgary.ca
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Our research participants travel to us from Calgary and the surrounding area. Please reach out, as we will work with you to support rural participation in our trials.
We are open for important research that provides medical care to patients living with chronic diseases.
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