Key Insights

Highlights

Success Rate

85% trial completion

Research Maturity

60 completed trials (48% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 52/100

Termination Rate

8.9%

11 terminated out of 124 trials

Success Rate

84.5%

-2.0% vs benchmark

Late-Stage Pipeline

10%

13 trials in Phase 3/4

Results Transparency

15%

9 of 60 completed with results

Key Signals

9 with results85% success11 terminated

Data Visualizations

Phase Distribution

77Total
Not Applicable (58)
P 1 (3)
P 2 (3)
P 3 (3)
P 4 (10)

Trial Status

Completed60
Recruiting23
Unknown16
Terminated11
Not Yet Recruiting7
Withdrawn4

Trial Success Rate

84.5%

Benchmark: 86.5%

Based on 60 completed trials

Clinical Trials (124)

Showing 20 of 20 trials
NCT07705269Not ApplicableRecruiting

The FILTRATE Trial: High-Rate Ultrafiltration for Intravascular Congestion

NCT07627360Not ApplicableNot Yet Recruiting

PRO STRESS Trial: Proactive Low-Dose Norepinephrine to Reduce Intraoperative Fluid Administration in Patients at High-Risk for Postoperative Pulmonary Complications Undergoing Laparoscopic Abdominal Surgery

NCT07643597Recruiting

Volume Removal Intolerance During Net Ultrafiltration in Acute Kidney Injury Patients

NCT05318105Not ApplicableTerminated

Ultrafiltration Versus IV Diuretics in Worsening Heart Failure

NCT07626151Not ApplicableRecruiting

Electric Cardiometry-Guided Standard Versus Restricted Fluid Therapy In Robotic Prostaectomy

NCT04180397Phase 4RecruitingPrimary

Controlled Fluid Removal in Critical Ill Patients With Fluid Overload in the Intensive Care Unit.

NCT07070973Not ApplicableRecruiting

Proactive Hemodynamic Management During Cytoreductive Surgery and HIPEC

NCT07541768Not ApplicableRecruiting

Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment.

NCT06823115Enrolling By Invitation

Assessment of Worldwide Acute Kidney Injury Epidemiology in Neonates 2.0

NCT04608149Active Not Recruiting

Prospective, Multi-center, Single-arm, Observational Study. US FDA 522 Pediatric Post Market Surveillance Study.

NCT06167707Phase 1Completed

Pharmacokinetics and Pharmacodynamics of Subcutaneous vs Intravenous Furosemide in Healthy Volunteers

NCT06995144Phase 4Completed

Comparing Natriuretic Effects of ER Torsemide to IR Torsemide in Patients With Heart Failure

NCT07178470RecruitingPrimary

Concordance and Discordance in the Assessment of Volume Status in Home Dialysis Patients: A Comparison of Modified Medical Research Council Dyspnea Scale, Physical Exam, and Point of Care Ultrasound (POCUS)

NCT07275658RecruitingPrimary

Timing and Dose of Fluid Deresuscitation in Critically Ill Patients

NCT07077772Not ApplicableRecruiting

Natriuresis-guided Depletion After Cardiac Surgery

NCT05817539Not ApplicableRecruiting

Early Deresuscitation Strategy Driven by Tissue Perfusion in Renal Replacement Therapy in Patients With Acute Renal Failure

NCT04914455Completed

Transhepatic Echography for Fluid Responsiveness After Cardiovascular Surgery

NCT05505500RecruitingPrimary

Interview Study of Adult and Child Patients and Parents of Children With Swelling Due to Nephrotic Syndrome.

NCT05188092Not ApplicableRecruiting

Lung Ultrasound-Guided Fluid Deresuscitation in ICU Patients

NCT05957003Not ApplicableCompletedPrimary

Fluid Responsiveness in Post-cardiac Surgery

Scroll to load more

Research Network

Activity Timeline