Search clinical trials for: PrePex™ device

Total 10046 results

Ministry of Health and Child Welfare, Zimbabwe

Completed

Comparing the PrePex™ Device to Surgical MC for Rapid Scale Up of MC in Resource Limited Setting

HIV

Zimbabwe
Ministry of Health, Rwanda

Completed

Comparing the PrePex™ Device to Surgical Circumcision for Rapid Scale Up of Male Circumcision in Resource Limited Setting

HIV

Rwanda
Ministry of Health, Rwanda

Completed

Cohort Field Study to Assess the Safety and Efficacy of the PrePex Device for Non-Surgical Circumcision When Performed by Nurses

HIV Prevention | Male Circumcision

Rwanda
Ministry of Health and Child Welfare, Zimbabwe

Completed

Evaluation of Safety and Efficacy of the PrePexTM Device for Rapid Scale up of Adult MC Programs in Zimbabwe (ZW-01)

HIV Infections | Circumcision Adult | HIV CDC Category B2

Zimbabwe
Ministry of Health and Child Welfare, Zimbabwe

Completed

Safety and Efficacy of the PrePex Device Circumcision When Performed by Nurses

Circumcision Adult | HIV CDC Category B2

Zimbabwe
Ministry of Health, Rwanda

Completed

Safety Study of the PrePex Device for Non-Surgical Adult Male Circumcision During Phased in National Implementation in an Effort to Prevent the Spread of HIV (RMC-07)

Male Circumcision

Rwanda
Ministry of Health, Rwanda

Completed

Follow Up Study to Evaluate a Non-Surgical Device for Adult Male Circumcision for Screen Failure Subjects (RMC-05)

HIV Prevention | Male Circumcision | Screen Failure Subjects | Narrow Foreskin

Rwanda
University of Washington
Centers for Disease Control and Prevention; University of Zimbabwe; Ministry... and other collaborators

Completed

Evaluation of the PrePex Device for Rapid Scale-up of VMMC, Phase 3 Field Implementation Trial With HIV + Adult Males

HIV Seropositivity

Zimbabwe
FHI 360
University of Illinois at Chicago; Bill and Melinda Gates Foundation; Nyanza... and other collaborators

Completed

Observational Study of Male Circumcision Using PrePex Device

HIV

Kenya
Assistance Publique - Hôpitaux de Paris

Unknown

ACT™ Balloons Versus Artificial Urinary Sphincter (AMS800™) for the Treatment of Female Stress Urinary Incontinence (SU-ACT)

Urinary Incontinence

France
Ministry of Health, Rwanda

Unknown

Safety and Efficacy Study of Non-Surgical MC Device for Adolescent Male Population Including Contraindicated Subjects

Circumcision, Adolescents

Rwanda
Ministry of Health, Rwanda
Ministry of Defence, Rwanda

Completed

A Pivotal Study to Assess the Safety and Efficacy of The PrePex System, a Male Circumcision Device and Methodology for Rapid Scale up of Painless and Bloodless National Circumcision Programs, in Urban and Remote Rural Settings

HIV Infections | HIV Prevention | Male Circumcision

Rwanda
Medtronic Neurovascular Clinical Affairs

Completed

Prospective Study on Embolization of Intracranial Aneurysms With Pipeline™ Embolization Device (PREMIER)

Intracranial Aneurysm

United States, Canada
Medtronic Neurovascular Clinical Affairs

Recruiting

EvaLuate EndoVascular Treatment of Acutely Ruptured Shallow Intradural Aneurysms With the Pipeline™ Flex Embolization Device With Shield TEchnology™ (ELEVATE) (ELEVATE)

Intracranial Aneurysm | Ruptured Aneurysm

United States
Smart Medical Systems Ltd.

Completed

Safety and Efficacy of Using NaviAid™ BGE Device (Balloon Guided Endoscopy) For Endoscopic Diagnosis and Treatment

Intestinal Diseases

United Kingdom
Medtronic Neurovascular Clinical Affairs

Completed

SOLITAIRE™ FR With the Intention For Thrombectomy (SWIFT) Study (SWIFT)

Ischemic Stroke

United States
Spokane Joint Replacement Center

Completed

Femoral Remodeling Following Total Hip Arthroplasty With OMNI Apex Modular™ and OMNI Apex ARC™ Stem Compared to Competitive Designs

Osteoarthritis, Hip

United States
Evasc Medical Systems Corp.

Withdrawn

Canadian eCLIPs™ Safety and Feasibility Study Protocol (CESIS)

Intracranial Aneurysms

Canada
Centre Hospitalier Intercommunal Creteil
Seven Dreamers Europe SAS

Recruiting

Efficacy of an Intranasal Stent on Nasal Obstruction at Night (RHINASTENT)

Nasal Obstruction

France
Firstkind Ltd

Completed

A Study in Patients With Venous Leg Ulcers and Measuring the Effects of Using Geko™ Device

Venous Leg Ulcer

United Kingdom
Becton, Dickinson and Company

Completed

A 7 Day Adhesive Device Wear Study to Evaluate BD StatLock™ Devices

Peripheral Intravenous Catheter Stabilization

United States
CorAssist Cadiovascular Ltd.

Recruiting

CORolla® TAA for Heart Failure With Preserved Ejection Fraction (HFpEF) and Diastolic Dysfunction (DD)

Diastolic Heart Failure | Diastolic Dysfunction

Israel
Vascutek Ltd.
Federation of Medical Specialties

Active, not recruiting

The Study of the Fenestrated Anaconda Device in the Treatment of Abdominal Aortic Aneurysms (EPI-EFA)

Vascular Diseases | Aneurysm

France
Vivasure Medical Limited

Completed

Safety and Performance Study of Large Hole Vascular Closure Device (FRONTIER-II)

Percutaneous Common Femoral Artery Arteriotomy Closure

Germany, United Kingdom, Ireland, Belgium
University of Oregon

Recruiting

The Validity of CORE Sensor in Heat Training for Male and Female Endurance Athletes (CORE)

Temperature Change, Body

United States
Boston Scientific Corporation

Recruiting

A 5-year Superion™ IDS Clinical Outcomes Post-Approval Evaluation (SCOPE)

Lumbar Spinal Stenosis

United States
Jeffrey A. Gusenoff, MD

Completed

Validation of a Novel Foot Offloading Device (PopSole2)

Heel Pain Syndrome | Plantar Fasciitis, Chronic | Fat Pad Syndrome

United States
Firstkind Ltd

Completed

Efficacy Study for Geko Device in VLU Patients

Leg Ulcer | Venous Leg Ulcer | Wound | Wound Leg | Leg Ulcers Venous

United Kingdom
Cynosure, Inc.

Completed

Feasibility Study To Collect Safety And Preliminary Efficacy Data For A Radiofrequency Microneedling Device

Acne Scars | Wrinkles | Fine Lines | Enlarged Pores | Crepey Skin | Loose Skin | Active Acne

United States
Becton, Dickinson and Company

Completed

Prospective Healthy Volunteer Study of the Securis™ Stabilization Device

Peripheral Intavenous Catheter Stabilization

United States
American Medical Systems

Completed

Global Performance Evaluation of the AMS CONTINUUM™ Device

Prostate Cancer

Spain, Greece
CorAssist Cadiovascular Ltd.

Unknown

CORolla™ TAA for Heart Failure and Preserved Ejection Fraction and Diastolic Dysfunction

Diastolic Heart Failure NYHA Class III-IV | Diastolic Dysfunction Secondary to Aortic Stenosis

Italy
Dr. Harindra Wijeysundera
Medtronic; Mars Excellence in Clinical Innovation and Technology Evaluation

Terminated

A Study of Renal Denervation in Patients With Treatment Resistant Hypertension (PaCE)

Treatment-Resistant Hypertension

Canada
Medtronic Neurovascular Clinical Affairs

Recruiting

Artisse™ Intrasaccular Device IDE (ARTISSE)

Intracranial Aneurysm

United States
American Medical Systems

Completed

Performance Evaluation of the AMS CONTINUUM™ Device

Prostate Cancer

United States
Medtronic Neurovascular Clinical Affairs
ev3 International

Completed

Solitaire FR Thrombectomy for Acute Revascularisation (STAR)

Stroke, Acute

Switzerland
KarmelSonix Ltd.

Completed

Wheeze Detection in Children During Dynamic Bronchial Situations Measured by WIM-PC™ Recording

Asthma, Bronchial

Israel
Blue Note Therapeutics
Curebase Inc.

Active, not recruiting

Virtual Trial to Compare Two Digital Therapeutics as Interventions for Physical and Mental Health in People With Cancer (RESTORE)

Cancer

United States
Medtronic Neurovascular Clinical Affairs
Medtronic Bakken Research Center

Completed

Pipeline Flex With SHield Technology Embolization - An International MulticEnter ObservationaL Post Market StuDy (SHIELD)

Intracranial Aneurysm

United Kingdom, Denmark, Israel, France, Spain, Germany, Greece, Australia, Finland, Hungary, Italy
Texas Tech University Health Sciences Center
MedHab, LC

Terminated

Comparative Effectiveness of an Activity-specific Monitoring Device- StepRite

Osteoarthritis | Degenerative Joint Disease

United States
Medtronic Neurovascular Clinical Affairs

Active, not recruiting

Pipeline™ Vantage Embolization Device With Shield Technology™ for Wide-Necked Intracranial Aneurysms (ADVANCE) (ADVANCE)

Intracranial Aneurysm

United States
Firstkind Ltd
National Institute for Health Research, United Kingdom; University of California and other collaborators

Recruiting

GEKO Venous Thromboembolism Prevention Study

Deep Vein Thrombosis | Venous Thromboembolism | Stroke, Acute | Pulmonary Embolism

United Kingdom
Cedars-Sinai Medical Center

Active, not recruiting

Trial to Compare the SherpaPak™ Device vs Cold Storage (SherpaPak)

Organ Transplant

United States
Neurent Medical

Completed

Safety and Efficacy Study of the Neurent Medical NEUROMARK™ System in Subjects With Chronic Rhinitis (MERIDIEN)

Chronic Rhinitis

United States
Paul Ong

Unknown

Feasibility Trial Evaluating Efficacy and Safety of Solitaire™ Thrombus Retrieval Device in the Management of Refractory Thrombus in Patients With Acute Coronary Syndrome (Solitaire)

Refractory Thrombus in Patients With Acute Coronary Syndrome

Singapore
Eduardo Schiffer
University Hospital, Geneva; Insel Gruppe AG, University Hospital Bern

Not yet recruiting

Platelet Count and Function After Usage of Two Different Cell Saver Devices During Liver Transplant Surgery (PLFLTS)

Liver Transplant | Hemorrhage, Surgical

Switzerland
Masimo Corporation

Enrolling by invitation

Impact of Bridge™ Device to Treat Opioid Withdrawal Symptoms

Opioid Use Disorder

United States
Medical University of Vienna
LSI SOLUTIONS, Inc.

Recruiting

Mi-STITCH™ and Mi-KNOT™ Device Technologies - Improvement of Mitral Valve Repair

Mitral Regurgitation | Mitral Valve Insufficiency

Austria
Tissium

Active, not recruiting

TISSIUM's Nerve Coaptation Device First-in-Human Clinical Trial

Digital Nerve Injury

Australia
Medtronic - MITG

Completed

Cytosponge Adequacy Study Evaluation II (CASEII)

GERD | Barrett's Esophagus

United States

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