Trial · NCT06269484
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cumulative Number of Subjects With Any of the Components of the Composite Endpoint: >2kg Increase in Body Weight (Office-based), >2 L Increase in Total Body Water, Increase in 2 or More Loop-diuretic Equivalents, Fluid Retention Adverse Event (AE) | baseline to Week 6 | Cumulative number of subjects with event of composite fluid retention endpoint |
| Secondary | Change From Baseline in Body Weight | at Week 6 | Change in site body weight |
| Secondary | Change From Baseline in Body Fat Mass | at Week 6 | |
| Secondary | Change From Baseline in Total Body Water | at Week 6 | |
| Secondary | Change From Baseline in Extracellular Water Volume | at Week 6 | |
| Secondary | Change From Baseline in Intracellular Water Volume | at Week 6 | |
| Secondary | Change in Body Weight (kg) Over Time Course of Study | at Week 6 | Change in home body weight |
| Secondary | Change in Total Dosage of Loop-diuretic Equivalents Use | at Week 6 | One loop-diuretic equivalent = 40 mg furosemide = 1 mg bumetanide = 20 mg torsemide = 50 mg ethacrynic acid. In Japan, one loop-diuretic equivalent = 40 mg furosemide = 8 mg torsemide = 60 mg azosemide. |
| Secondary | Cumulative Number of Subjects With Either of the Two Components of This Composite: 1. >3 L Increase in Total Body Water Volume From Baseline to Week 6 2. Increase in 3 or More Loop-diuretics Equivalents Use | from baseline to Week 6 | Cumulative number of subjects with event of composite and the components of total body water and total dosage of loop-diuretic equivalents |
| Secondary | Absolute Change in Systolic Blood Pressure | at Week 6 | |
| Secondary | Absolute Change in Diastolic Blood Pressure | at Week 6 |
Source ClinicalTrials.govtrials-2026-11-12-0.4.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT06269484/registered