Trial · NCT06036914
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 14 of 14
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Urine Output | 24 hours | The total volume of urine produced in milliliters (mL) over 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Body Weight | Baseline, 24 hours | Change in Body Weight (kg) from Baseline to 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in NT-proBNP | Baseline, 24 hours | Change in NT-proBNP levels (pg/ml) from Baseline to 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Urine Sodium Excretion | Baseline, 24 hours | Change in amount of sodium (mmol) excreted in the urine from Baseline to 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Apnea-hypopnea Index | Baseline, 24 hours | The apnea-hypopnea index (AHI) is the number of apneas and hypopneas per hour of sleep which is an indicator of severity of sleep apnea AHI will be measured using a Watch Pat or Nox device at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Iohexol Glomerular Filtration Rate (GFR) | Baseline, 24 hours | Renal or kidney function was measured by GFR determined by Iohexol clearance. Iohexol GFR will be measured at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Peripheral Vein Pressure | Baseline, 24 hours | Peripheral vein pressure (mm Hg) will be recorded from existing IV lines through pressure transducer monitoring at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Cardiac Output | Baseline, 24 hours | Cardiac output (L/min) is the total volume of blood moved by the heart per minute and will be measured by echocardiography conducted at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Estimated Right Ventricular (RV) Systolic Pressure | Baseline, 24 hours | Estimated RV systolic pressure (mm Hg) will be measured by echocardiography conducted at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Right Atrial (RA) Pressure | Baseline, 24 hours | RA pressure (mm Hg) will be measured by echocardiography conducted at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Left Atrial (LA) Strain | Baseline, 24 hours | LA strain will be assessed by echocardiography conducted at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Left Ventricular (LV) Global Longitudinal Strain | Baseline, 24 hours | LV global longitudinal strain will be assessed by echocardiography conducted at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in Right Ventricular (RV) Global Longitudinal Strain | Baseline, 24 hours | RV global longitudinal strain will be assessed by echocardiography conducted at Baseline and 24 hours after initiation of intravenous diuretic. |
| Secondary | Change in E/e' | Baseline, 24 hours | E/e' will be assessed using echocardiography conducted at Baseline and 24 hours after initiation of intravenous diuretic. It is defined as the ratio of peak early diastolic mitral inflow velocity (E) and peak early diastolic mitral annular velocity (e'). |
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.
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GET https://conductscience.org/api/trials/v1/NCT06036914/registered