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Trials / Conditions / Chronic Venous Insufficiency, CVI

Chronic Venous Insufficiency, CVI

12 registered clinical trials studyying Chronic Venous Insufficiency, CVI5 currently recruiting.

StatusTrialSponsorPhase
Not Yet RecruitingThe ReCAna for Lower ExtremIty Venous OBstructions and In-StEnt Restenosis Registry
NCT07529756
Intervene, Inc.
Not Yet RecruitingEfficacy and Safety of Endovenous Ablation for Relief of Knee Pain in Elderly Patients With Lower Extremity Va
NCT07239284
Chengdu University of Traditional Chinese Medicine
RecruitingRisks and Benefits of Radiofrequency Ablation for Chronic Venous Insufficiency (CEAP C3-C6) in Patients Aged 8
NCT07233616
Chengdu University of Traditional Chinese Medicine
Not Yet RecruitingKnee Pain Relief After Endovenous Treatment for Lower Limb Varicose Veins: A Prospective Observational Study
NCT07163312
Chengdu University of Traditional Chinese Medicine
RecruitingReducing Skin Tone Inequities in Chronic Venous Insufficiency
NCT06798766
King's College London
CompletedFirst- or Second- Class Compression Hosiery After Endovenous Laser With Sclerotherapy and Ambulatory Phlebecto
NCT06913764
Moscow City Hospital named after A.K. EramishantsevN/A
Active Not RecruitingSafety of the Sonablate HIFU System for the Ablation of Incompetent Veins of the Periphery
NCT06642051
SonablateN/A
CompletedRespiratory Functions, Aerobic Capacity and Quality of Life in Chronic Venous Insufficiency
NCT06785805
Izmir Democracy University
CompletedAdding a Combined Program of Therapeutic Exercise and Self-massage to the Conventional Approach of Compression
NCT06727968
University of ValenciaN/A
TerminatedInvestigation of Femoropopliteal In Situ Valve Formation With the InterVene System (INFINITE-US)
NCT04225806
Intervene, Inc.N/A
CompletedClinical Study to Assess the Safety and Efficacy of Mechanochemical Ablation With Flebogrif in Patients With G
NCT04558957
Balton Sp.zo.o.N/A
CompletedEfficacy on Volume Reduction and Tolerance of Progressiv' Medical Compressive Therapy (MCT) V0322 BC in Patien
NCT01402921
Pierre Fabre MedicamentPhase 3