Search clinical trials for: OMNI® Surgical System

Total 3960 results

Iqbal Ahmed
OMNI Medical Services, LLC

Terminated

Standalone OMNI Surgical System for Open-angle Glaucoma (OMNIgl)

Open Angle Glaucoma

Canada
Sight Sciences, Inc.

Terminated

A Prospective, Multicenter Study of the OMNI® Surgical System in Pseudophakic Eyes With Open Angle Glaucoma (ORION)

Glaucoma, Open-Angle

United States
Sight Sciences, Inc.

Completed

An Observational Multicenter Clinical Study To Assess The Safety And Effectiveness Of The OMNI® Surgical System In Pseudophakic Eyes With Primary Open Angle Glaucoma (ORION 2.0)

Glaucoma, Open-Angle

United States
Sight Sciences, Inc.

Terminated

A Post-market Study Of Use Of The OMNI® Surgical System In Open Angle Glaucoma

Glaucoma, Open-Angle

United States
Sight Sciences, Inc.

Terminated

Study of OMNI Surgical System and iStent for Eyes With OAG (Trident)

Glaucoma, Open-Angle

Germany, Spain, United Kingdom
Mark Gallardo, MD

Unknown

A Single Center Proof Of Concept Study To Assess Intra And Perioperative Safety Profile Of OMNI Surgical System

Open Angle Glaucoma

United States
Sight Sciences, Inc.

Completed

A Clinical Study To Assess The Safety And Effectiveness Of The OMNI® Surgical System

Glaucoma, Open-Angle

United States
Sight Sciences, Inc.

Not yet recruiting

A Clinical Trial Comparing the OMNI Surgical System to Standard Medical Treatment in Pseudophakic Eyes (EVOLVE)

Primary Open Angle Glaucoma

United States
Nova Eye, Inc.
Nova Eye Medical GmbH

Recruiting

Multicenter Glaucoma Study Investigating Standalone Canaloplasty (MAGIC)

Primary Open Angle Glaucoma

United Kingdom, Germany, Spain
New World Medical, Inc.

Not yet recruiting

An Extension Trial for Patients With Open-Angle Glaucoma Who Participated in the DF6-CL-20-01 Protocol.

Intraocular Pressure | Open Angle Glaucoma

Costa Rica
Nova Eye, Inc.

Terminated

Multicenter Ab-interno Glaucoma Study Investigating Canaloplasty (MAGIC)

Primary Open Angle Glaucoma

United States
Kinderwunsch Institut GmbH
Institut AllergoSan

Completed

Influence of Probiotics on the Vaginal Microbiota

Vaginal Microbiome

Austria
Endoscopic Technologies, Inc

Terminated

Efficacy and Safety Study of the Estech COBRA® Surgical System to Treat Patients With a History of Irregular Heart Beats

Persistent Atrial Fibrillation

United States
Azienda Ospedaliera Universitaria Integrata Verona

Recruiting

Comparison of Outcomes of Multiple Platforms for Assisted Robotic - Gastrectomy

Neoplasms | Gastric Cancer | Gastrointestinal Cancer | Gastric Neoplasm | Stomach Adenocarcinoma | Gastric Diffuse Adenocarcinoma

Italy
AtriCure, Inc.

Recruiting

Inappropriate Sinus Tachycardia Registry

Postural Tachycardia Syndrome | Inappropriate Sinus Tachycardia

Belgium
AtriCure, Inc.

Enrolling by invitation

Tracking Results of Ablations to Combat AF Registry (TRAC-AF)

Atrial Fibrillation
Sofregen Medical, Inc.

Terminated

SERI® Surgical Scaffold Postmarket Study of Soft Tissue Support in Ventral Hernia Repair

Ventral Hernia Repair

United States
University of Pennsylvania

Completed

Transoral Robotic Surgery (TORS) for Sleep Apnea

Obstructive Sleep Apnea

United States
Integra LifeSciences Corporation

Completed

T-GENVIH-003 LTFU (Long Term Follow Up) Study

Hernia | Pathological Conditions, Anatomical | Hernia, Abdominal | Hernia, Ventral

United States
Azienda Ospedaliera Universitaria Integrata Verona

Recruiting

Comparison of Outcomes of Multiple Platforms for Assisted Robotic - Prostate (COMPAR-P)

Prostate Cancer

Italy
Sofregen Medical, Inc.

Completed

The SeriScaffold® Use in Reconstruction Post Market Study for Tissue Support and Repair in Breast Reconstruction Surgery in Europe

Soft Tissue Support and Repair

Spain, Germany, United Kingdom, Italy
Sofregen Medical, Inc.

Completed

SERI® Surgical Scaffold for Soft Tissue Support in Revision Augmentation Surgery

Subjects Requiring Revision Breast Augmentation Surgery

United States
Sofregen Medical, Inc.

Completed

The SERI® Surgical Scaffold Use in Reconstruction Post Market Study for Tissue Support and Repair in Breast Reconstruction Surgery

Breast Reconstruction

United States
The Methodist Hospital Research Institute

Terminated

The Use of CoSeal (Sealant Agent) in Patients During Left Ventricular Assist Device Surgery

Heart Failure | Ventricular Dysfunction

United States
Alcon Research

Completed

Clinical Comparison of 27+® and 23-gauge ULTRAVIT® 7500 Cpm Vitrectomy Outcomes

Vitreoretinal Disease

United States
Cairo University

Completed

Surgicel Reduces Ovarian Endometriomas Recurrence

Endometrioma

Egypt
Cairo University

Unknown

Surgicel® & Endometrial Ablation in the Management of Perimenpausal Heavy Menstrual Bleeding

Endometrial Hyperplasia

Egypt
Göteborg University

Completed

PHS, Lichtenstein Mesh, and PerFixPlug for Primary Inguinal Hernia Repair - 3 Years Results (BOOP)

Hernia, Inguinal

Sweden
Aesculap AG

Completed

Trial to Evaluate the Hemostatic Effect of Lyostypt® Versus Surgicel® in Arterial Bypass Anastomosis (COBBANA)

Peripheral Vascular Diseases | Hemostasis

Germany
Intuitive Surgical

Completed

IS-001 Injection Phase-1 Safety, Tolerance and Pharmacokinetics

Surgery | Hysterectomy

United States
Arthrex, Inc.

Recruiting

Knee Related Subchondral Bone Lesions Treated With IOBP (IOBP)

Subchondral Cyst

United States
University Hospital, Bordeaux
Ministry for Health and Solidarity, France

Completed

Total Disc Replacement Versus Anterior Cervical Decompression and Fusion (CERVIDISC)

Cervical Degenerative Disc Disease

France
Medtronic Cardiovascular

Completed

Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Symptomatic Severe Aortic Stenosis in High Risk and Very High Risk Subjects Who Need Aortic Valve Replacement

Severe Aortic Stenosis

United States
Alyatec
Medicom

Completed

Efficacy of Face Mask in Reducing Respiratory Allergic Symptoms in Birch-allergic Subjects in ALYATEC Exposure Chamber

Allergic Rhinitis | Allergic Asthma

France
Medical University of Warsaw

Completed

Study to Evaluate DACC Dressings for the Prevention of Surgical Site Infections in Women Undergoing Caesarean Section.

Surgical Site Infection | Infection; Cesarean Section

Poland
pfm medical ag
Aix Scientifics; Crolll Gmbh; Bayes GmbH; GfE Medizintechnik GmbH; pfm medical titanium...

Completed

Anterior Pelvic Prolapse Reconstruction With TiLOOP® Total 6

Cystocele | Uterine Prolapse

Germany
Ohio State University Comprehensive Cancer Center

Recruiting

Transoral Robotic Surgery in Treating Patients With Benign or Malignant Tumors of the Head and Neck

Tongue Cancer | Recurrent Squamous Cell Carcinoma of the Hypopharynx | Recurrent Squamous Cell Carcinoma of the Larynx | Recurrent Squamous Cell Carcinoma of the Lip and Oral Cavity | Recurrent Verrucous Carcinoma of the Larynx | Recurrent Verrucous Carcinoma of the Oral Cavity | Recurrent Adenoid... and other conditions

United States
University Maribor

Completed

The Multistrain Probiotic OMNi-BiOTiC® Active for Upper Respiratory Tract Infections in Older People (ProURTI)

Acute Upper Respiratory Tract Infection

Slovenia
Medtronic Cardiovascular

Completed

Concomitant Utilization of Radio Frequency Energy for Atrial Fibrillation (CURE-AF) Study

Atrial Fibrillation

United States
Medtronic Cardiovascular

Active, not recruiting

Safety and Efficacy Study of the Medtronic CoreValve® System in the Treatment of Severe, Symptomatic Aortic Stenosis in Intermediate Risk Subjects Who Need Aortic Valve Replacement (SURTAVI). (SURTAVI)

Severe Aortic Stenosis

United States, Netherlands, Canada, Spain, Denmark, United Kingdom, Switzerland, Germany, Sweden
Cohera Medical, Inc.

Terminated

A Clinical Study Comparing Standard Anastomosis Closure Technique to Standard Closure Techniques Plus Sylys® Surgical Sealant

Colorectal and Ileorectal Anastomosis | Colocolic and Ileocolic Anastomosis | Coloanal and Ileoanal Anastomosis

United States
University Health Network, Toronto

Not yet recruiting

Assessment of Oxygen Delivery as an Early Predictor of Postoperative Pulmonary Complications During One-lung Pulmonary Ventilation in Thoracic Surgery. A Pilot Study (DO2 and POPCs)

Postoperative Pulmonary Complications
Permed Biomedical Engineering Co., Ltd
Changhai Hospital; Shanghai Zhongshan Hospital; Southwest Hospital, China; West... and other collaborators

Enrolling by invitation

The Branch-based Intraoperative Stent System in the Treatment of Stanford A Aortic Dissection（BROAD） (BROAD)

Cardiovascular Diseases | Vascular Diseases | Aneurysm | Aneurysm, Dissecting | Aortic Dissection

China
Medtronic Cardiac Surgery

Completed

Medtronic Concomitant Utilization of Radio Frequency for Atrial Fibrillation CURE-AF/Persistent (CURE-AF/Perst)

Atrial Fibrillation

United States
China Medical University, China

Completed

Traumastem® Versus Surgicel® for the Secondary Treatment of Local Bleeding in Patients Undergoing Hepatic Resection (TSFHR)

Liver Hemorrhage

China
Takeda
Baxter Healthcare Corporation

Completed

Comparison of Efficacy and Safety of TachoSil® Versus Surgicel® Original for the Secondary Hemostatic Treatment of Needle Hole Bleeding in Vascular Surgery (VASUS)

Bleeding

United States
Medtronic Cardiovascular

Completed

European CURE-AF Study

Atrial Fibrillation

Germany, Norway, Poland
M.D. Anderson Cancer Center

Completed

Robotic Harvest of the Latissimus Dorsi (LD) Muscles

Cancer | Complications | Surgical Procedure, Unspecified | Other Reconstructive Surgery | Failure of Muscle Graft

United States
Mayo Clinic

Recruiting

Robotic Surgery in the Seated Position for Benign and Malignant Lesions of the Head and Neck

Head and Neck Cancer | Oropharyngeal Neoplasms

United States
Takeda

Completed

TachoSil® Versus Surgicel® Original for the Secondary Treatment of Local Bleeding in Adult and Pediatric Patients Undergoing Hepatic Resection Surgery

Hemorrhage

United States

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