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Procedural Complication clinical trials

View clinical trials related to Procedural Complication.

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NCT ID: NCT05115591 Completed - Anesthesia Clinical Trials

Ultrasound Predictors of Difficult Spinal Anesthesia

SPINAL-US
Start date: March 5, 2021
Phase:
Study type: Observational

This prospective observational study aims to investigate about the efficacy of spine ultrasound in predicting difficult spinal anesthesia

NCT ID: NCT04235790 Completed - Clinical trials for Procedural Complication

Examining Behaviors of Teachers of Invasive Bedside Procedures Using an Eye Tracking Device

Start date: October 30, 2020
Phase: N/A
Study type: Interventional

Researchers are studying the behaviors in teachers of invasive bedside procedures to improve the safety of invasive bedside procedure in the Intensive Care Unit (ICU).

NCT ID: NCT04076605 Completed - Bleeding Clinical Trials

Bleeding in Hospitalized Patients With Liver Disease Undergoing Invasive Procedures

PROC-BLeeD
Start date: November 15, 2019
Phase:
Study type: Observational

Patients with cirrhosis are frequently hospitalized and often undergo procedures. Knowledge surrounding bleeding risk is sparse and practice patterns vary across centers in regards to bleeding prophylaxis. The goal of this study to is to obtain more knowledge regarding risk factors for procedural related bleeding in patients with cirrhosis and to develop a predictive model to risk stratify patients before undergoing procedures. Through collaboration from centers across the world this study should provide information on prevalence of bleeding and variation in practice patterns for prophylaxis.

NCT ID: NCT03645213 Completed - Nursing Caries Clinical Trials

Two Different Distraction Methods on Pain and Fear During Venipuncture in Children

Start date: September 18, 2017
Phase: N/A
Study type: Interventional

Objective: Needle-related procedures (venipuncture, vaccine injections) are the most common source of pain and fear, and generally experienced in childhood for the first time. This study was designed to determine the effects of watching cartoon films on non-VR and VR virtual reality on pain and fear during venipuncture in school-age children and to compare these two methods. Method: This randomized controlled trial study was conducted on 120 school-age children (7 -12 years of age) with pain and fear of venipuncture. The children were randomized according to their arrival in the biochemistry laboratory; the first, second, and third children were assigned VR distraction group with a headset (n=40), non-VR distraction group on a tablet computer screen (n=40) and no distraction group (n=40), respectively. The data collection was carried out using the children identification form, Wong-Baker FACES Pain Rating Scale evaluating the pain and Childrens' Fear Scale evaluating the fear. The outcomes reported by the children, parent, and observer.

NCT ID: NCT03462745 Completed - Clinical trials for Procedural Complication

A Comparison of the First Attempt Success Rate of Cannulation Between the Accuvein Apparatus and Standard Technique

Start date: February 10, 2013
Phase: N/A
Study type: Interventional

Background: The AccuVein AV300 device helps in venepuncture and intravenous (IV) cannulation. It uses infrared light that can be absorbed by the blood hemoglobin so that veins location is clearly viewed on the skin's surface. Objectives: To assess the effectiveness of the AV300 device over the standard technique in increasing the first-time success rate (SR) for pediatric patients who needed IV cannulation. Methods: This was a prospective cross study of patients aged 0-18 years scheduled for surgery or examination under anesthesia but without having an existing IV access and after providing consent form. Patients were randomized into two groups; cannulation with AV300 or standard insertion performed by experienced pediatric anesthesiologists and residents under training.