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Surgery clinical trials

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NCT ID: NCT04277299 Completed - Surgery Clinical Trials

Intelligent Customer-driven Solution for Children and Their Parents Undergoing Day Surgery

Start date: August 12, 2020
Phase: N/A
Study type: Interventional

This research aims to evaluate the effectiveness of web-based mobile intervention (Icory -Solution) developed to pediatric patients and their parents in the pathway of outpatient surgery treatment in pre-intra- and postoperative setting: (1) Examine the effectiveness of the intervention on children's preoperative anxiety and fear, and postoperative pain (2) examine the effectiveness of the intervention on parental anxiety and satisfaction in children´s care path and (3) examine the experiences of the gamification in children in the intervention group.

NCT ID: NCT04276831 Completed - Surgery Clinical Trials

Comparison Between Laryngoscope McCoy With Macintosh

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

This study aimed to compare cardiovascular response and ease of intubation using laryngoscope McCoy with Macintosh

NCT ID: NCT04274491 Completed - Surgery Clinical Trials

Predictors of Recovery Expectancy

Start date: March 1, 2020
Phase:
Study type: Observational

The purpose of this study is to identify factors that influence a person's expectations regarding recovery from pelvic organ prolapse surgery. This is important because a person's expectations regarding recovery from surgery help to predict how a person will actually recover. Our hypothesis is that women with multiple roles will have expectations of a longer surgical recovery time after surgery for pelvic organ prolapse after controlling for known predictors of recovery expectancies. Participants will complete a preoperative online survey. Additional online surveys will be send on postoperative days 14 and 42 to measure postdischarge surgical recovery.

NCT ID: NCT04271098 Completed - Surgery Clinical Trials

The Investigation of the Causes of Hepatic Dysfunction in the Postoperative Period During Open-heart Surgeries

Start date: January 1, 2012
Phase:
Study type: Observational [Patient Registry]

In a prospective observational study during the six-month duration, coronary artery bypass graft surgery (CABG) and valve repair surgery (mitral, mitral, and aortic valve and/or tricuspid valve) patients were investigated for hepatic dysfunction. All patients were divided into two groups as with or without hyperbilirubinemia, and this was defined by the occurrence of a plasma total bilirubin concentration of more than 34 µmol/L (2 mg/dL) in any measurement during the postoperative period. Our goal was to determine the risk factors associated with hepatic dysfunction in patients undergoing open-heart surgery with cardiopulmonary bypass. The collected parameters include; alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP), total bilirubin (TBIL), and gamma-glutamyl transpeptidase (GGT) and albumin preoperatively and on postoperative days 1, 3 and 7. Possible preoperative, intraoperative, and postoperative risk factors were investigated. Logistic regression analysis was done to identify the risk factors for postoperative hyperbilirubinemia.

NCT ID: NCT04269421 Completed - Surgery Clinical Trials

Return To Sport Activities in Patients Surgically Treated For Flat Foot in Paeditric Age

CSSPORT
Start date: March 1, 2020
Phase:
Study type: Observational [Patient Registry]

The SURGERY of arthrosis of the subtalar joint, carried out between 9 and 12 years of age, the aim is to restore and maintain the physiological alignment between the talus and the calcaneus during bone maturation. There are few articles in the literature that talk about the return to sport of pediatric patients after surgery. The aim of the study is to review patients operated on remotely kick heel and describe how they return in their sports (resilience, type of activities carried out, recovery times). The aim of this study is to evaluate the clinical and functional results of patients of age Pediatric treated in the investigator's SC Orthopedics Pediatric Traumatology department for flat feet with "calcaneostop" surgery. The study aims to describe the method of resuming sports activities, analyzing the timing and difficulties declared by patients after surgery, with the help of specific questionnaires.

NCT ID: NCT04261699 Completed - Surgery Clinical Trials

One-stage Adjustable Strabismus Surgery Under AIVOC

AIVOC
Start date: January 28, 2020
Phase:
Study type: Observational

The purpose of this study is to note that one-stage adjustable surgery can be enough to provide satisfactory results for the correction of strabismus in adults thanks to the use of an anesthesia type AIVOC (Target-controlled infusion of Propofol-Remifentanyl)

NCT ID: NCT04252833 Completed - Surgery Clinical Trials

Open-label, Crossover, Food Effect Study to Evaluate CT-044 in Healthy Human Volunteers

Start date: February 18, 2020
Phase: Phase 1
Study type: Interventional

This open-label study will be conducted to assess the bioavailability and PK of oral single doses of CT-044 following administration with and without food and to evaluate the safety and tolerability of CT-044 when given with and without food.

NCT ID: NCT04252469 Completed - Surgery Clinical Trials

Efficacy of Pre-intubation Chlorhexidine Oral Care on Health Outcomes

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

This single-centre, single-blind, randomised controlled study with parallel-group design was conducted in Yun Ling, Taiwan between May 2019 and August 2019. Participants were randomly allocated to an intervention (mouth care using 0.12% CHX before intubation) or control (standard care) group on a 1:1 basis. This study was approved by the institutional review board of National Taiwan University Hospital, Taiwan (IRB No.201806086RINB). Each participant completed written informed consent after explanation of this study and advised that they could withdraw anytime.

NCT ID: NCT04251637 Completed - Surgery Clinical Trials

Non Invasive Cardiac Output Evaluation With Starling SV for Lung Elective Surgery

NICOLE
Start date: September 25, 2020
Phase:
Study type: Observational

Intraoperative hemodynamic optimization decreases postoperative complications and length of stay in high risk patient. Therefore, continuous monitoring of cardiac output (Qc) is recommended to guide fluid management. Thoracic bio-reactance is a recent technique that allows cardiac output non-invasive monitoring. However, additional clinical validation studies in humans are required to better define the typologies of patients for whom this monitoring could be proposed routinely. Lung surgery is defined as an intermediate or high risk surgery regarding postoperative cardiac complications. However, surgical patients rarely benefit from continuous monitoring of cardiac output, the available methods being considered too invasive or insufficiently reliable in daily practice. Thoracic bio-reactance (Non Invasive Cardiac Output Monitor (NICOM) Starling SV) has not been studied in this subgroup of clinically relevant patients.

NCT ID: NCT04246099 Completed - Surgery Clinical Trials

Opioid-free Anesthesia in Thoracic Surgery

VATOFA
Start date: March 1, 2019
Phase:
Study type: Observational

No study has been conducted to demonstrate the feasibility and safety of an Opioid-Free Anesthesia (OFA) protocol compared to Opioid-Based Anesthesia (OBA) in thoracic surgery, at risk for intense post-operative pain, to improve patient care. The aim of the present study was to evaluate the effect of OFA on post-operative opioids consumption, pain and the post-operative period after lobectomy by Video-Assisted Thoracoscopy Surgery (VATS). systems. Investigators perform a retrospective, single-center study in 2019. Patients were divided into two groups: OFA (with dexmedetomidine) or OBA (sufentanyl). Investigators analyse the total postoperative opioid consumption in the 48 h after surgery. Investigators asses pain intensity in the 48 h after surgery, operative hemodynamic stability, Post-Operative Pain (POP) in Post-Anesthesia Care Unit (PACU) and POP on day 30. All data are available in the medical record Hypothesis: OFA can reduce post-operative opioids consumption, pain in lobectomy by video-assisted thoracoscopy surgery (VATS).