Clinical Trials Sponsored by JOTEC Company

Total 6075 results

University Hospital, Ghent
JOTEC Company

Completed

Multicentric, Prospective, Randomized, Comparing Trial Between Bypass of the Femoropoplitea by PTFE and Heparin Bounded PTFE

Peripheral Vascular Diseases

Belgium
JOTEC GmbH

Recruiting

A PMCF Study in Patients With Thoracoabdominal Aortic Aneurysms Treated With E-nside TAAA Multibranch Stent Graft System (INNER-B-APAC)

Thoracoabdominal Aortic Aneurysm

New Zealand, Thailand, Australia
JOTEC GmbH

Recruiting

A Post-Market Clinical Follow-up Study in Patients Treated With Vascular Grafts (FLOWGRAFT)

Vascular Diseases

Germany
JOTEC GmbH

Terminated

E-tegra Stent Graft System in the Treatment of Infra-renal Abdominal Aortic Aneurysms (SECURE)

Abdominal Aortic Aneurysm | AAA

France, Germany, Spain, Poland, Switzerland
JOTEC GmbH

Recruiting

A PMCF Study in Patients With Infrarenal Aortic Aneurysm Treated With the E-tegra Stent Graft System (EASY)

Vascular Aneurysm

Netherlands
JOTEC GmbH

Recruiting

A Study in Patients With Thoracoabdominal Aortic Aneurysm Treated With the E-nside TAAA Multibranch Stent Graft System (INNER-B)

Vascular Aneurysm

Germany
JOTEC GmbH

Recruiting

Post-market Registry of the AMDS for the Treatment of Acute DeBakey Type I Dissection (PROTECT)

Aortic Dissection | Intramural Hematoma | Acute DeBakey I Dissection | Acute Type A Dissection

Germany
JOTEC GmbH

Active, not recruiting

Post Market Clinical Follow-Up Study in Patients Treated With the On-X Ascending Aortic Prosthesis (AAP) (ASCEND)

Aortic Valve Disease

United States, Spain, United Kingdom, Germany, Italy
JOTEC GmbH

Active, not recruiting

PMCF Study in Patients With Acute or Chronic Aortic Dissection or Aortic Aneurysm Treated With E-vita OPEN NEO (NEOS-APAC)

Aortic Aneurysm | Aortic Dissection

Thailand, Singapore, Hong Kong, Korea, Republic of, Malaysia, Australia
JOTEC GmbH

Active, not recruiting

Registry in Patients With Thoracoabdominal Aneurysms (CONNECT)

Thoracoabdominal Aneurysm

Germany
JOTEC GmbH

Recruiting

EASYII - E-tegra Stent Graft System - Imaging Cohort (EASYII)

Vascular Aneurysm

Netherlands
JOTEC GmbH

Recruiting

Registry in Patients With Aorto-iliac or Iliac Aneurysms (PLIANTII)

Vascular Aneurysm

Germany
JOTEC GmbH

Active, not recruiting

A PMCF Study in Patients With Acute or Chronic Aortic Dissection or Aortic Aneurysm Treated With E-vita OPEN NEO (NEOS)

Aortic Aneurysm | Aortic Dissection

Austria, Germany
JOTEC GmbH

Active, not recruiting

Prospective Multicenter Study for the Endovascular Treatment of Iliac Aneurysm With the Branched E-liac Stent Graft (TAILOR)

AAA | Iliac Aneurysm

France
JOTEC GmbH

Completed

Prospective/Retrospective Registry of the E-vita OPEN PLUS Stent Graft System in France (FEOR)

Vascular Diseases

France
JOTEC GmbH

Completed

Post-market Registry in Patients With Iliac Aneurysm Undergoing Endovascular Stenting With the E-liac Stent Graft System

Iliac Aneurysm

Germany, Spain, Poland, Austria
JOTEC GmbH

Completed

A Study in SurvIvors of Type B Aortic Dissection Undergoing Stenting (ASSIST)

Type B Aortic Dissection

Germany, Spain, Poland, Italy
JOTEC GmbH
ICON plc

Recruiting

French Registry Conducted on E-vita OPEN NEO (NEO)

Vascular Aneurysm

France
JOTEC GmbH
MedPass International

Recruiting

A Study in Patients With Complicated Type B Aortic Dissection Treated With the E-nya Thoracic Stent Graft (CONFORM-TAD)

Vascular Diseases

Germany
JOTEC GmbH
MedPass International

Recruiting

A Study in Patients With a Descending TAA or PAU Treated With the E-nya Thoracic Stent Graft System (CONFORM-TAA)

Vascular Aneurysm

Germany
Botec Analysis, LLC

Unknown

An Evaluation of the NJSPB SCF Project for Opioid-Involved High-Risk Parolees

Substance Abuse | Criminal Behavior

United States
Perrigo Company

Completed

Bioequivalence Study Between Two Oral Formulations of Famotidine Tablets Under Fasting Conditions

Bioavailability
Perrigo Company

Completed

Bioequivalence Study Between Two Oral Formulations of Naproxen 500 mg Tablets Under Fasting Conditions

Bioequivalency
Perrigo Company

Completed

Bioequivalence Study Between Two Oral Formulations of Famotidine Tablets Under Fed Conditions

Bioavailability
Genome & Company

Not yet recruiting

A First-in-human Study of GENA-104A16 in Patients With Advanced Solid Tumors

Advanced Solid Tumors

Korea, Republic of
OBMedical Company

Completed

Electrode-Based Sensor for Non-Invasive Fetal Heart Rate Monitoring With Improved Reliability (FHR)

Laboring Women With Ultrasound and FSE Monitoring

United States
Perrigo Company

Completed

Bioequivalence Study Between Two Oral Formulations of Ibuprofen 800 mg Tablets Under Fasting Conditions

Bioequivalency
Perrigo Company

Completed

Bioequivalence Study Between Two Oral Formulations of Ibuprofen 800 mg Tablets Under Fed Conditions

Bioequivalency
Perrigo Company

Completed

Bioequivalence Study Between Two Oral Formulations of Naproxen 500 mg Tablets Under Fed Conditions

Bioequivalency
Botec Analysis, LLC
Pennsylvania Department of Corrections; Bureau of Justice Assistance

Unknown

Swift, Certain, and Fair: Reducing Recidivism and Improving Outcomes for Alcohol and Drug Users on State Parole

Substance Abuse | Criminal Behavior
DynPort Vaccine Company LLC, A GDIT Company

Completed

A New Anthrax Vaccine Administered by the Intramuscular (IM) Route in Healthy Adults

Anthrax

United States
DynPort Vaccine Company LLC, A GDIT Company

Withdrawn

Safety, Tolerability and Immunogenicity of the Venezuelan Equine Encephalitis (VEE) Attenuated Live-Virus Vaccine

Venezuelan Equine Encephalitis

United States
DynPort Vaccine Company LLC, A GDIT Company

Completed

Study to Evaluate the Safety, Tolerability and Immunogenicity of Recombinant Botulinum Vaccine A/B in Healthy Adults

RECOMBINANT BOTULINUM VACCINE A/B

United States
DynPort Vaccine Company LLC, A GDIT Company

Completed

Double Blind, Safety and Immunogenicity Study of Recombinant Botulinum Vaccine A/B

Botulism Vaccine

United States
DynPort Vaccine Company LLC, A GDIT Company

Completed

Randomized Single-Blinded Study to Evaluate Safety and Immunogenicity of Recombinant Plague Vaccine With and Without Adjuvant

Plague Vaccine

United States
DynPort Vaccine Company LLC, A GDIT Company

Withdrawn

Phase 3, Randomized, Safety, Lot Consistency and Clinical Benefit Study of Recombinant Botulinum Vaccine A/B (rBV A/B)

Botulism
DynPort Vaccine Company LLC, A GDIT Company

Completed

Title: Recombinant Plague Vaccine rF1V in Healthy Volunteers

Healthy Volunteers

United States
DynPort Vaccine Company LLC, A GDIT Company

Completed

Safety, Tolerability & Immunogenicity of the Recombinant Plague Vaccine rF1V

Pneumonic Plague | Preventive Therapy

United States
DynPort Vaccine Company LLC, A GDIT Company

Completed

Study of Reactogenicity, Safety, Immunogenicity, and Pock Lesion Formation of a Cell-Cultured Smallpox Vaccine Compared to Dryvax®

Smallpox

United States
University of California, San Francisco
Mahidol University; Holley-Cotec Pharmaceuticals Co., LTD.

Completed

Pharmacokinetics of Dihydroartemisinin-Piperaquine in the Treatment of Uncomplicated Malaria in Children in Burkina Faso

Uncomplicated Malaria
RAI Services Company

Not yet recruiting

CSD231005 Nicotine Pouch Biomarkers of Exposure

Smoking | Tobacco Use

United States
Balmoral Medical company

Recruiting

A Study to Evaluate the Safety and Effectiveness Transdermal Compress Device in Participants With Transfemoral Amputations

Prosthesis and Implants

United States
Kowa Company, Ltd.

Recruiting

A Phase 3 Study to Evaluate the Efficacy and Safety of K-877 in Chinese Patients With High TG and Low HDL-C

Hyperlipidemia

China
BrainScope Company, Inc.

Recruiting

Follow-up of mTBI Patients Discharged From the ED Using Standard Clinical Triage Including BrainScope One (MEDO)

TBI (Traumatic Brain Injury) | Concussion, Brain | MTBI - Mild Traumatic Brain Injury | Closed Head Injury

United States
Kowa Company, Ltd.

Completed

A Phase III Confirmatory Study of K-237

Covid19

Japan, Thailand
RAI Services Company

Completed

CSD200902: Assessment of Indoor Air Quality for a Heated Tobacco Product With Four Non-Combusted Cigarette Variants in an Environmental Testing Chamber

Smoking | Tobacco Use | Tobacco Smoking

United States
The Medicines Company

Completed

Study to Evaluate the Safety, Tolerability and Pharmacokinetics of a New Formulation of Oritavancin in Healthy Volunteers

Healthy

United States
Kowa Company, Ltd.

Completed

K-924 Phase III Confirmatory Study

Hypercholesterolemia

Japan
RAI Services Company

Completed

BRP1602: Evaluation of Technical and Logistical Feasibility to Measure Lung Permeability

Smoking | Tobacco Use | Smoking, Tobacco

United States
RAI Services Company

Completed

CSD201301: Study to Assess Elements of Abuse Liability for Four P13 Nicotine Pouches

Smoking | Tobacco Use | Tobacco Smoking

United States

3

Subscribe