Rapid and Simultaneous Initiation of Four Guideline-Directed CKD Therapies (RAPID-CKD)
Part of paid clinical trials in Temple, Texas.
- Sponsor
- Baylor Research Institute
- Study ID
- NCT07547878
- Phase
- PHASE4
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 84 Years
- Healthy Volunteers
- Not accepted
Interventions
- Finerenone — DRUG10-40mg daily
- Semaglutide — DRUG.25-1.0mg 1 time a week
- Lotensin — DRUG10-40mg daily
- Capoten — DRUG12.5-50mg 3 times a day
- Enalapril — DRUG2.5-10mg daily
- Monopril — DRUG10-40mg daily
- Lisinopril — DRUG5-20mg daily
- Univasc — DRUG3.75-15mg daily
- Aceon — DRUG4-16mg daily
- Accupril — DRUG10-40mg daily
- Altace — DRUG1.25-5mg daily
- Mavik — DRUG1-4mg daily
- Edarbi — DRUG40-80mg daily
- Atacand — DRUG8-32mg daily
- Avapro — DRUG150-300mg daily
- Cozaar — DRUG25-100mg daily
- Benicar — DRUG20-40mg daily
- Micardis — DRUG20-80mg daily
- Diovan — DRUG80-320mg daily
- Invokana — DRUG100mg daily
- Farxiga — DRUG10mg daily
- Jardiance — DRUG10mg daily
- Ertugliflozin — DRUG5mg daily
- Brenzavvy — DRUG20mg daily
- Sotagliflozin — DRUG200-400mg daily
Study Details
The goal of this clinical trial is to learn if starting four kidney disease medicines quickly and together (a rapid treatment approach) is safe and works well in people with type 2 diabetes and chronic kidney disease. The main questions it aims to answer are: * Is it safe to start these medicines over a short period of time? * How often do kidney function changes or high potassium levels occur? * Does this approach lower protein in the urine (a sign of kidney damage)? * How many participants are able to stay on all four medicines over 6 months? Researchers will compare this approach to usual care, where medicines are started one at a time over several months. Participants will: Be assigned by chance to either this approach or usual care Start up to four approved kidney medicines over about 8 weeks (rapid treatment approach) or follow standard care Have regular clinic visits and lab tests to check kidney function and potassium levels Be followed for about 6 months
Key Dates
- Start date
- Apr 30, 2026
- Status verified
- Apr 2026
- Primary completion
- Mar 31, 2029
- Completion
- Mar 31, 2029
Study Design
- Enrollment
- 64 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Interventional GroupSubjects receive all four chronic kidney disease therapies (medications) at the same time.
- Active Comparator: Control GroupSubjects received standard of care
Primary Outcome Measure
On-study retention rate at 6 months [ Time Frame: 6 months ]
Central Contacts
- Shahzeb Khan, MD469-326-2636
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Baylor Scott and White Medical Center- Temple | Temple | Texas | 76508 | Shahzeb Khan, MD (PRINCIPAL_INVESTIGATOR) |
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