Clinical trials: Device Success Rate
Vascular Access Complications
Comparison of AccuCath IV Catheter and Conventional IV Catheter in Interventional Radiology
The study will test a hypothesis that the AccuCath™ System will have a higher rate of successful first attempt peripheral IV placement and higher clinician and patient satisfaction compared to Conventional IV Catheters.
- Trial name
- NCT01940354
- Testing
- AccuCath IV Catheter System, Conventional IV Catheter System
- Where
- United States
- Volunteers
- 220 people, healthy volunteers welcome
- Sponsor
- C. R. Bard
Vascular Access Complication
AccuCath Guidewire Intravenous (IV) Device Versus Conventional IV Catheter In General Nursing Use
The study will test a hypothesis that the AccuCath™ System will have a higher rate of successful first attempt peripheral intravenous (IV) placement, higher completion of therapy, fewer complications, longer dwell times, and…
- Trial name
- NCT01943474
- Testing
- AccuCath IV Catheter Device, Conventional IV Catheter Device
- Where
- United States
- Volunteers
- 248 people
- Sponsor
- C. R. Bard
Benzodiazepine Withdrawal
Can Connected Devices Increase the Success Rate of Benzodiazepine Withdrawals in the Elderly?
This is a prospective randomized open study, which aims to evaluate the benefit of a connected watch to help people aged 65 years and older to withdraw from BZD over a six-month period, compared with classical withdrawal (e.g…
- Trial name
- BENZO-E-STOP (NCT04912479)
- Testing
- connected watch
- Where
- France
- Volunteers
- 100 people
- Sponsor
- University Hospital, Toulouse
Respiratory Insufficiency, Intubation
Retrospective Data Analysis With the Aim to Determine the Success Rate of Endotracheal Intubation in the First Attempt in the Zug Rescue Service With Various Airway Devices Already in Everyday Use
Airway management is a critical procedure in emergency medicine, especially endotracheal intubation, which can be life-saving. Various techniques, such as video laryngoscopes and conventional laryngoscopes, are used, with success…
- Conditions
- Respiratory Insufficiency, Intubation, Airway Management, Prehospital Airway Management in Patients With Cardiac Arrest
- Trial name
- AWARE (NCT06653166)
- Testing
- bougie (S Guide), videolaryngoscopy
- Where
- Switzerland
- Volunteers
- 200 people
- Sponsor
- Rettungsdienst Zug
Vascular Access Complication
AccuCath™ Intravenous (IV) Device Used by Vascular Access Team (VAT)
The study will test a hypothesis that the AccuCath™ System will have a higher rate of successful first attempt peripheral intravenous (PIV) placement, higher completion of therapy, fewer complications, longer dwell times, and…
- Trial name
- NCT01937195
- Testing
- AccuCath Intravenous Catheter System
- Where
- United States
- Volunteers
- 95 people
- Sponsor
- C. R. Bard
Device Success Rate, Device Performance
The i-GelTM. A Randomized, Crossover Study With the Laryngeal Mask Airway ProSealTM in Anesthetized Pediatric Patients
In the following randomized, crossover study, the investigators test the hypothesis that ease of insertion and oropharyngeal leak pressure differ between the LMA ProSealTM and the i-GelTM in anesthetized pediatric patients.
- Trial name
- NCT01425151
- Testing
- i-Gel, ProSeal
- Where
- 2 sites in Austria, Switzerland
- Volunteers
- 60 people
- Sponsor
- Schulthess Klinik
Cardiac Arrest (CA)
Does Increasing the Compression Pause From 3 to 5 Seconds in Mechanical Compression Devices Increase Ventilation Success Rate and Return of Spontaneous Circulation?
To give chest compressions during cardiopulmonary resuscitation (CPR), mechanical chest compression devices can be used. During synchronous 30:2 CPR, the standard setting on these devices leave an automated 3-second chest…
- Trial name
- LUCASVP (NCT06824961)
- Testing
- 5-second ventilation pause duration during mechanical CPR, 3-second ventilation pause duration during mechanical CPR
- Where
- 2 sites in Netherlands
- Volunteers
- 692 people
- Sponsor
- Amsterdam UMC, location VUmc
External Ear Disorder
A Clinical Trial to Test the Saftey and Success Rate for a Cerrumen Cleaning Device - "Wondertip".
Wondertip is a silicone single use device with a coil end, designed for the purpose of evacuating impacted cerumen of external ear canals. This trial aims at testing the safety and efficacy of this device.
- Trial name
- NCT03019380
- Testing
- removing cerumen from external ear (Wondertip)
- Volunteers
- 50 people
- Sponsor
- Kaplan Medical Center
Anesthesia Intubation Complication, Difficult Intubation
Safety and Efficacy of Cleverscope. A New Medical Device for Tracheal Intubation
Cleverscope is a new medical device that transform a laryngoscope into a videolaryngoscope. previous its commercialization we evaluate its safety and efficacy.
- Trial name
- NCT03902704
- Testing
- Cleverscope, Laryngoscope / Videolaryngoscope C-MAC® Storz
- Where
- Spain
- Volunteers
- 134 people
- Sponsor
- Hospital General Universitario de Valencia
Ascites Hepatic
Comparison Between Conventional Angiocatheter Versus New Anchoring Device (KARAHOC) Used for Paracentesis
Comparison of success rate and complication between conventional angiocatheter versus new anchoring device (KARAHOC) used for paracentesis in cirrhotic patients with ascites.
- Trial name
- NCT05578573
- Testing
- KARAHOC device, Angiocatheter
- Where
- South Korea
- Volunteers
- 80 people
- Sponsor
- Sang Gyune Kim
Evaluation of Success Rate, Airway Leak Pressure
Evaluation of Supraglottic Airway Devices in Children and Comparison to Historic Control
The supraglottic airway device LMA Supreme has recently been introduced for pediatric patients. The investigators will prospectively evaluate success rate and airway leak pressure in everyday's clinical pediatric anesthesia…
- Conditions
- Evaluation of Success Rate, Airway Leak Pressure, Side Effects of LMA Supreme in Pediatric Patients Undergoing General Anesthesia
- Trial name
- NCT01625858
- Where
- Switzerland
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- Insel Gruppe AG, University Hospital Bern
Supraglottic Airway Device, Intubation; Difficult or Failed
Effect of Head-neck Rotation on I-gel™ Insertion
According to previous studies, head and neck rotation reduces the tongue from being rolled back by gravity, which resulted in increasing patency of the upper airway.
- Conditions
- Supraglottic Airway Device, Intubation; Difficult or Failed, Airway Complication of Anesthesia
- Trial name
- NCT05201339
- Testing
- Standard method, Hean and Neck Rotation
- Where
- South Korea
- Volunteers
- 172 people
- Sponsor
- Seoul National University Hospital
Cannulation
A Comparison of the Success Rate Of Cannulation Between The Accuvein Apparatus And Standard Technique
1. This study will compare the first attempt success rate of cannulation in research participants randomized to using a new FDA approved AccuVein AV300 device for intravenous access with research participants randomized to…
- Trial name
- NCT01042613
- Testing
- Cannulation using Accuvein device, Standard Cannulation method
- Where
- United States
- Volunteers
- 146 people
- Sponsor
- St. Jude Children's Research Hospital
Intubation, General Anesthesia
Does the Use of the GlideRite® Endotracheal Tube in Combination With the I-gel® Improve Intubation Success Rate?
The investigators aim to compare two different types of supraglottic devices for tracheal intubation in patients undergoing elective surgery under general anesthesia.
- Trial name
- NCT01265862
- Testing
- Tracheal intubation through LMA-Fastrach®, Tracheal intubation through I-gel®
- Where
- Canada
- Volunteers
- 120 people
- Sponsor
- Centre hospitalier de l'Université de Montréal (CHUM)
Sleep Apnea, Obstructive
Obstructive Sleep Apnea - Patient Specific Factors, Success Rate and Compliance
Obstructive sleep apnea (OSA) is a condition where the patient's breathing cease during sleep due to collapse of the oro-pharynx.
- Trial name
- NCT02953028
- Testing
- CPAP, Mandibular Advancing Splint
- Where
- 2 sites in Norway
- Volunteers
- 119 people
- Sponsor
- University of Tromso
Peripheral Vascular Access in Pediatric Patients, Peptic Ulcer
The Effect of Vascular Imaging Devices on Success Rates of Peripheral Vascular Access in Pediatric Patients
The study was designed as a prospective, observational study. Pediatric patients under 18 years of age scheduled for peripheral vascular access placement during day-case surgery or non-operating room anesthesia (NORA) will be…
- Conditions
- Peripheral Vascular Access in Pediatric Patients, Peptic Ulcer, Cataract, Crohn's Disease
- Trial name
- NCT07315711
- Where
- 6 sites in Turkey (Türkiye)
- Volunteers
- 500 people
- Sponsor
- Sibel Seçkin Pehlivan
Surgical Operation With Implant of Artificial Internal Device
A Non-Interventional Study to Document the Use of Straumann BLX Implants in Daily Dental Practice
Prospective, multi-center, non-interventional observation to document the success and survival rates of Straumann BLX Implants used for tooth replacement in cleared indications up to 1 year after implant placement
- Trial name
- BLX_NIS (NCT03613077)
- Testing
- surgical placement of an endosteal implant
- Where
- Germany
- Volunteers
- 153 people
- Sponsor
- Institut Straumann AG