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NCT ID: NCT05619003 Completed - Clinical trials for Pressure Injury Prevention

Biatain Silicone Sacral for Pressure Injury Prevention in Hospital-admitted Patients at Risk

Start date: August 26, 2022
Phase: N/A
Study type: Interventional

A post market clinical follow-up study investigating the safety of Biatain Silicone Sacral while used as prevention in hospital admitted patients at risk of developing a pressure injury.

NCT ID: NCT05618106 Completed - Clinical trials for Irritable Bowel Syndrome

Low FODMAP Diet in Patients With IBS

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

The aim was aimed to investigate if all carbohydrate groups eliminated in the Low FODMAP diet are equally important in relieving gastrointestinal symptoms in IBS. in a randomized cross-over design to three different carbohydrate-modified diets: A) Low Polyol diet, B) Low FOS+GOS diet, and C) Low FODMAP diet for three months without wash-out-periods. Gastrointestinal symptoms, Quality of life was measured at baseline and after each intervention diet.

NCT ID: NCT05615909 Completed - Prostate Cancer Clinical Trials

PRO-MR-RT Systematic Patient-reported Outcomes to Pelvic Online MRgRT

Start date: November 19, 2020
Phase:
Study type: Observational

In 2018 the Unity MR-linac was approved for treating patients with online magnetic resonance (MR)-guided radiotherapy. With the MR-linac it is possible to get real-time MR images with high soft tissue contrast, adapt the radiotherapy plan and subsequently irradiate at each treatment fraction. Patients with prostate cancer is one of the patient groups referred for this new treatment and potentially they will benefit with decreased margins around the tumour and increased local tumor control rates. The acute toxicity is important when evaluating treatment tolerability. A prospective longitudinal observation of the acute treatment toxicity to online MR-guided radiotherapy is therefore essential in the evaluation of this new technology. Patient-reported outcomes (PRO) are disease symptoms and treatment toxicity reported directly by patients themselves without clinician interpretation. Several studies have indicated that clinicians tend to underreport the incidence and severity of patient symptoms, thus a systematic use of PROs in clinical trials can provide valuable evidence to the clinicians. As online MR-guided radiotherapy (MRgRT) is a new technology there is limited research worldwide on patient-reported symptoms and quality of life. The objective of this study is therefore to prospectively investigate the patient-reported acute toxicity and changes in quality of life during and after online MR-guided radiotherapy.

NCT ID: NCT05610254 Completed - Clinical trials for Hemodynamic Instability

The Cold Fluids Study

Start date: October 24, 2022
Phase: Phase 4
Study type: Interventional

In this single center crossover study the aim is to investigate the effect of Ringer's lactate solution at high and low temperatures on physiological response in healthy adults.18 healthy volunteers will be included. Inclusion criteria is; Age between 18-64. Exclusion criteria is; Pre-existing medical problems, Pregnancy (validated through a certified pregnancy test), Body mass index >35 kg/m2, Medication use apart from allergy medication, contraceptives, or non-steroidal anti-inflammatory drugs. Participants will be randomized to receive 30 ml/kg of Ringer's lactate either cold (15°C, 59°F), or at body temperature (37°C, 98.6°F) during a 30-minute interval. Fluids will be administered through a peripheral vein. After a minimum "washout period" of 24 hours, subjects are switched to receive infusion at the other aforementioned temperatures. Primary outcome is - The increase in MAP at 15 minutes after infusion of the fluid bolus. Secondary outcome is - Time until return of MAP to baseline value after infusion.

NCT ID: NCT05607485 Completed - Clinical Competence Clinical Trials

Laypersons Cannot Select Preferred Surgeon Based on Videos of Simulated Robot-assisted Radical Prostatectomies

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The goal of this comparative blinded assessment study is to compare ratings of crowd workers and expert ratings in simulated robot-assisted radical prostatectomies The main question[s] it aims to answer are: - to examine the use of crowdsourced assessment for assessing the performance of robot-assisted rad-ical prostatectomy (RARP) compared with using experienced surgeons - to explore if some CW are better than others. Participants will assess edited videos of simulated robot assisted radical prostatecotmies using a standardized assessment tool. The laypersons will be asked to answer yes/no to the question: 'Would you trust this doctor to perform robot-assisted surgery on you?' after each surgery. All participants were blinded to the identity of the surgeon performing the videos of the robot-assisted radical prostatectomy Researchers will compare laypersons with expert raters to see if any difference between their ratings

NCT ID: NCT05604313 Completed - Ergonomics Clinical Trials

The Effects of Using an Ergonomic Chinrest When Playing the Violin

Start date: January 4, 2021
Phase: N/A
Study type: Interventional

A one-day crossover randomised trial was conducted to compare violinists using an ergonomic chinrest (EC) with do-as-usual on muscle activation, kinematics and sound. After two weeks of testing the EC, self-perceived evaluations on comfort, performance, sound, neck alignment and muscle tension were reported in a questionnaire between EC and do-as-usual. The main question is to answer if: 1. the EC is superior compared to do-as-usual and gives a more aligned neck posture and less muscle tension/dynamic muscle activity 2. the EC is subjectively evaluated as better than do-as-usual regarding self-perceived comfort, performance and sound

NCT ID: NCT05601765 Completed - Orthopaedic Surgery Clinical Trials

The Effect of Digital Team-based Communication on Patient-initiated Telephone Contacts to Hospital After Discharge

Start date: October 31, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effects of eDialogue versus standard communication pathways on patient-initiated telephone contacts to the hospital following discharge. Secondary aims are to explore the effect on other patient-initiated contacts after hospital discharge (mail, video, SMS, personal attendance) and, if digital team-based communication can positively affect patients experience of continuity of care.

NCT ID: NCT05601089 Completed - Stroke Clinical Trials

Inter-Tester Reliability Of the Cumulated Ambulation Score in Patients With Stroke (InTRO-CAS-stroke)

Start date: October 24, 2022
Phase:
Study type: Observational

CAS is a measurement of basic mobility describing the degree of independence in three activities; getting in and out of bed, sit-to-stand from a chair with armrests, and indoor walking - each assessed on a three-point ordinal scale (0-2), resulting in a total one-day CAS between 0-6 points. Psychometric properties of the CAS has not been investigated i stroke. The design is an inter-tester reliability study.

NCT ID: NCT05600530 Completed - Validation Study Clinical Trials

Validity and Reproducibility of Dietary Assessment Against Objective Measures

VALID
Start date: October 31, 2022
Phase:
Study type: Observational

A cross-sectional study with repeated measurements among healthy Danish adults to assess the validity and reproducibility of a self-administered 7-day web-based dietary assessment tool, myfood24® tested against objective biomarkers.

NCT ID: NCT05597657 Completed - Healthy Individuals Clinical Trials

Normal Variation of T1 Values With Cardiac Magnetic Resonance in Healthy Individuals

NATIVE
Start date: October 12, 2021
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the normal variation of T1 values with cardiac magnetic resonance in healthy individuals with respect to reproducibility, changes over time, and dependency on hydration status.