Trial · NCT06036914
Outcomes14
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 14 of 14
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Urine Output | 24 hours | mL | MEAN | |
| SECONDARY | Change in Body Weight | Baseline, 24 hours | kg | MEAN | |
| SECONDARY | Change in NT-proBNP | Baseline, 24 hours | pg/ml | MEAN | |
| SECONDARY | Change in Urine Sodium Excretion | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a results, no data was collected for this outcome measure. | ||
| SECONDARY | Change in Apnea-hypopnea Index | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a result, no data was collected for this outcome measure. | ||
| SECONDARY | Change in Iohexol Glomerular Filtration Rate (GFR) | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a result, no data was collected for this outcome measure. | ||
| SECONDARY | Change in Peripheral Vein Pressure | Baseline, 24 hours | Data was not collected for 1 subject in the Ultra-High dose diuretic group as the subject requested that peripheral vein pressure data not be collected on them. | mmHg | MEAN |
| SECONDARY | Change in Cardiac Output | Baseline, 24 hours | Data was not technically feasible to obtain for 3 subjects in the Ultra-High Dose diuretic group for this outcome measure. | L/min | MEAN |
| SECONDARY | Change in Estimated Right Ventricular (RV) Systolic Pressure | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a result, no data was collected for this outcome measure. | ||
| SECONDARY | Change in Right Atrial (RA) Pressure | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a result, no data was collected for this outcome measure. | ||
| SECONDARY | Change in Left Atrial (LA) Strain | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a result, no data was collected for this outcome measure. | ||
| SECONDARY | Change in Left Ventricular (LV) Global Longitudinal Strain | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a result, no data was collected for this outcome measure. | ||
| SECONDARY | Change in Right Ventricular (RV) Global Longitudinal Strain | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a result, no data was collected for this outcome measure. | ||
| SECONDARY | Change in E/e' | Baseline, 24 hours | Data for this outcome measure was not collected for any participants. Upon study initiation, this outcome measure was not technically feasible to obtain with existing staffing and was therefore not performed. As a result, no data was collected for this outcome measure. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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.
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GET https://conductscience.org/api/trials/v1/NCT06036914/outcomes