Key Insights

Highlights

Success Rate

96% trial completion (above average)

Published Results

16 trials with published results (12%)

Research Maturity

77 completed trials (56% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

2.2%

3 terminated out of 138 trials

Success Rate

96.3%

+9.8% vs benchmark

Late-Stage Pipeline

3%

4 trials in Phase 3/4

Results Transparency

21%

16 of 77 completed with results

Key Signals

16 with results96% success

Data Visualizations

Phase Distribution

68Total
Not Applicable (58)
P 1 (1)
P 2 (5)
P 3 (1)
P 4 (3)

Trial Status

Completed77
Unknown23
Recruiting21
Withdrawn5
Active Not Recruiting5
Terminated3

Trial Success Rate

96.3%

Benchmark: 86.5%

Based on 77 completed trials

Clinical Trials (138)

Showing 20 of 20 trials
NCT06133075Phase 2Completed

Using Mirabegron to Increase BP in Patients With POTS

NCT06526884Not ApplicableActive Not Recruiting

Quasi-Randomized Evaluation of the UCLA Next Day Clinic (NDC)

NCT06472375RecruitingPrimary

In Hospital 24 Hour Observation of Syncope Patients

NCT07118124Not ApplicableActive Not RecruitingPrimary

Pediatric Adhesion and New Dermal Approach Study

NCT07374263Recruiting

Do QT-Prolonging Drugs Cause Major Adverse Cardiac Events in Hospitalized Adults?

NCT05066347Not ApplicableRecruitingPrimary

REmote Cardiac MOnitoring of At-risk SYNCope Patients After Emergency Department Discharge -RCT

NCT06310707Not ApplicableTerminated

Arrhythmia Identification in Syncope Patients: ePatch® Versus 24h Holter

NCT04075084Recruiting

Observation of Clinical Routine Care for Patients With BIOTRONIK Implantable Cardiac Monitors (ICMs)

NCT02824822Recruiting

Genetic Markers of Cardiovascular Disease in Epilepsy

NCT05560126Not Yet RecruitingPrimary

Canadian Prehospital Syncope Risk Score (Prehospital CSRS)

NCT06854484Recruiting

AVEIR™ Leadless Pacemaker (LP) United Kingdom (UK) Registry

NCT00359203Phase 4CompletedPrimary

ISSUE3: International Study on Syncope of Uncertain Etiology 3

NCT00170261Phase 4CompletedPrimary

ELIAS: Early Loop-Recorder in Suspected Arrhythmogenic Syncope

NCT04755101Not ApplicableRecruiting

Efficacy of a Right-sided Ablation of the Anterior Ganglionated Plexus for Neurally Mediated Syncope

NCT01548352Active Not RecruitingPrimary

BAsel Syncope EvaLuation (BASEL IX) Study

NCT03974412Not ApplicableCompletedPrimary

Syncope Trial to Understand Tilt Testing Early or Recorders Study

NCT06503653Not ApplicableActive Not RecruitingPrimary

Creation of a Syncope Channel for Patients Admitted to the Emergency Department for Loss of Consciousness and Not Hospitalized: Etiological Predictivity (Before/After Study)

NCT03940066Not ApplicableCompleted

Evaluation of Ambulatory Monitoring of Patients After High-risk Acute Coronary Syndrome Using Two Different Systems: Biomonitor-2 and Kardia Mobile

NCT04533425CompletedPrimary

Practical Approaches to Care in Emergency Syncope

NCT04972071Not ApplicableRecruitingPrimary

SW-RCT Implementation of Canadian Syncope Risk Score Based Practice Recommendations

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Research Network

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