Key Insights

Highlights

Success Rate

92% trial completion (above average)

Research Maturity

60 completed trials (61% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

5.1%

5 terminated out of 98 trials

Success Rate

92.3%

+5.8% vs benchmark

Late-Stage Pipeline

16%

16 trials in Phase 3/4

Results Transparency

5%

3 of 60 completed with results

Key Signals

3 with results92% success

Data Visualizations

Phase Distribution

50Total
Not Applicable (30)
Early P 1 (1)
P 1 (1)
P 2 (2)
P 3 (6)
P 4 (10)

Trial Status

Completed60
Unknown17
Recruiting7
Terminated5
Not Yet Recruiting4
Withdrawn3

Trial Success Rate

92.3%

Benchmark: 86.5%

Based on 60 completed trials

Clinical Trials (98)

Showing 20 of 20 trials
NCT02193412Not ApplicableCompletedPrimary

Influence of Variations of Systemic Venous Return on Analgesia Nociception Index (ANI) During General Anaesthesia

NCT07492511Recruiting

Renal and Hepatic Abnormal Doppler Patterns in Trauma

NCT07435922Not Yet Recruiting

Evaluate Recombinant Human Serum Albumin From Oryza Sativa In Patients With Hypoalbuminemia and/or Hypovolemia Requiring Urgent Treatment

NCT06480942CompletedPrimary

Arterial Pressure Derived Dynamic Parameters to Detect Preload Responsiveness in Spontaneously Breathing Patients

NCT03592290RecruitingPrimary

Hemodynamics Monitoring During Lower Body Negative Pressure (LBNP) Induced Controlled Hypovolemia

NCT07192523Not ApplicableCompleted

Effects of Different Fluid Transfusion Regimens On Glycocalyx In Patients Undergoing Thoracic Surgery.

NCT07304648Not Yet Recruiting

Role of End-Tidal CO2 During Passive Leg Raising to Predict Fluid Responsiveness in ICU

NCT07304661Not Yet Recruiting

Comparison of PPV and LVOT VTI During Passive Leg Raising to Predict Fluid Responsiveness

NCT06231472Not ApplicableCompletedPrimary

Effect of Preoperative Fluid Therapy on Post-induction Hypotension

NCT07206732Not Yet Recruiting

IVC Ultrasound Versus Central Venous Pressure for Early Detection of Hypovolemia in Shock Patients

NCT01258361CompletedPrimary

Echocardiographic Assessment of Volume Variation Secondary to Preoperative Fasting

NCT06263075Recruiting

Hemodynamic Monitoring During Craniosynostosis Surgery: Comparing Traditional and Newer Technology Monitors (CRASY-PRAM)

NCT04186416RecruitingPrimary

Effectiveness of the Pressure Recording Analytical Method in Predicting Fluid Responsiveness in Pediatric Critical Care Patients

NCT02715466Phase 4TerminatedPrimary

Gelatin in ICU and Sepsis

NCT07108881Phase 4Completed

Ultrasound Guided Fluid Loading Before Spinal Anesthesia

NCT05931601Phase 3Recruiting

Early Initiated Vasopressor Therapy in the Emergency Department

NCT06072430Phase 3Recruiting

A Phase III, Open Label, Randomized, Controlled Study of VBI-S in the Treatment of Hypovolemia in Patients With Septic Shock (VBI-S-02)

NCT06123039Completed

Use of Heart-lung Interaction to Predict Haemodynamic Tolerance to the Open Lung Approach With Individualised PEEP

NCT02645851Not ApplicableTerminated

RApid Fluid Volume EXpansion in Patients in Shock After the Initial Phase of Resuscitation.

NCT06729268Completed

Fluid Responsiveness Tests in Critically Ill Patients During Admission to the Intensive Care Unit

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