Key Insights

Highlights

Success Rate

84% trial completion

Published Results

14 trials with published results (20%)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 39/100

Termination Rate

8.7%

6 terminated out of 69 trials

Success Rate

84.2%

-2.3% vs benchmark

Late-Stage Pipeline

17%

12 trials in Phase 3/4

Results Transparency

44%

14 of 32 completed with results

Key Signals

14 with results84% success

Data Visualizations

Phase Distribution

50Total
Not Applicable (35)
P 1 (2)
P 2 (1)
P 3 (3)
P 4 (9)

Trial Status

Completed32
Unknown21
Terminated6
Active Not Recruiting3
Recruiting3
Not Yet Recruiting2

Trial Success Rate

84.2%

Benchmark: 86.5%

Based on 32 completed trials

Clinical Trials (69)

Showing 20 of 20 trials
NCT06418282Not ApplicableRecruiting

Clinical Study to Evaluate the Effectiveness and Health Economics of a Novel Portable Non-Pneumatic Active Compression Device (NPCD) for Lymphedema/Phlebolymphedema

NCT03216005Not ApplicableTerminatedPrimary

Investigation of Femoropopliteal In Situ Valve Formation With the InterVene System

NCT04054440CompletedPrimary

Outpatient Office Based Endovascular Procedures

NCT05504070Not ApplicableActive Not Recruiting

Venclose digiRF System Post Market Study

NCT07449728Not ApplicableRecruiting

The Influence of Laser Crossectomy With Different Wavelengths on Varicose Vein Progression

NCT04897035Not ApplicableCompleted

Study to Evaluate the Safety and Effectiveness of Dayspring for Lower Extremity Lymphedema

NCT07390097Phase 4Not Yet Recruiting

Calcium Dobesilate After Radiofrequency Ablation for Varicose Veins

NCT06579482Phase 4CompletedPrimary

Clinical Trial of Aesculus Hippocastanum and Associations Versus Diosmina and Hesperidina in Chronic Venous Insuficiency

NCT05628688Completed

A Non-randomized, Open-Label Study to Evaluate the Safety and Effectiveness of Insight® Pro Device for Evaluating Lymphatic and Venous Disorders (VOLGA)

NCT05507346Not ApplicableCompleted

A Clinical Study to Evaluate the Effectiveness of a Novel Portable Non-Pneumatic Active Compression Device vs. an Advanced Pneumatic Compression Device for Treating Lower Extremity Lymphedema

NCT02462096Not ApplicableTerminatedPrimary

A Feasibility Study of the ReLeaf Catheter System

NCT05047302Not ApplicableWithdrawnPrimary

Investigation of Femoropopliteal In Situ Valve Formation With the InterVene System (INFINITE-Canada)

NCT06232421Phase 2Not Yet Recruiting

Clinical Study in Adult Patients With Purulent-inflammatory Processes of the Skin and Soft Tissues, Phase I-II of the Wound Process

NCT05622500Not ApplicableTerminatedPrimary

Best Endovenous Treatment, Including STenting, Versus Non-endovenous Treatment in Chronic Proximal Deep Venous Disease

NCT05926830Not ApplicableCompletedPrimary

Extracorporeal Flow Abolition in Relation With Primary Insufficiency of Great Saphenous Veins (GSV) Using High Intensity Focused Ultrasound (HIFU) Generated by Sonovein: A Multi Center Prospective Pivotal Study

NCT04231942Not ApplicableActive Not Recruiting

Elastic Compression Stockings and Varicose Veins Recurrence

NCT05982405Not ApplicableTerminatedPrimary

Long-term Effects of Inspiratory Muscle Training in Chronic Venous Insufficiency

NCT06196541Active Not RecruitingPrimary

Respiratory and Physical Functions in Individuals With Chronic Venous Insufficiency

NCT04580160Not ApplicableCompleted

Venous Stent for the Iliofemoral Vein Investigational Clinical Trial Using the DUO Venous Stent System

NCT05051540Not ApplicableCompletedPrimary

The Effect of Inelastic Compression System on Quality of Life in People With Chronic Venous Insufficiency

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