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NCT ID: NCT04934150 Completed - Chronic Pain Clinical Trials

Neuronavigated Repetitive Transcranial Magnetic Stimulation (nrTMS) of the Dorsolateral Prefrontal and Primary Motor Cortex for the Treatment of Chronic Pain

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

This study investigated the effects of navigated repetitive Transcranial Magnetic Stimulation on nociception and quality of life in patients suffering from chronic pain conditions. Two cortical targets (dorsolateral prefrontal cortex/DLPFC and M1 area) were stimulated and compared to Sham stimulation.

NCT ID: NCT04931186 Completed - Eye Diseases Clinical Trials

Nasolacrimal Duct Obstruction

Start date: July 3, 2018
Phase:
Study type: Observational

1.1 Background Obstructions of the lacrimal drainage system can be differentiated based on anatomical location or severity. But also, differentiating between congenital and acquired nasolacrimal duct obstruction (NLDO) is possible. The incidence of congenital NLDO (CNLOD) has been shown to be approximately 20%. Most of the cases undergo spontaneous remission, as the ductus nasolacrimalis may open spontaneously. About 2-12% display a symptomatic course. 2. S: 290; 3; 4, 5 Acquired NLDO may occur during childhood and adulthood. The incidence of symptomatic acquired NLDO is around 30 cases per 100.000 people in an US-based cohort study. S: 293; 30 Two major anatomical closure sites have been described, which are on the one hand located at the between the punctum and canaliculus, and on the other hand located after the lacrimal sac. 1. S. ; 2. S: 293 1.2 Aim of this study The aim of this study is to assess the success rates for different types of primary tear duct surgery, performed from 2013 - 2017 at the department of Ophthalmology and Optometry, Medical University of Vienna. Treatment success was defined as the absence of clinical signs of lacrimal drainage system obstruction (epiphora, increased tear leak, mucous discharge) and without the need for re-intervention. It is further investigated whether the type of operation performed or whether the silicone tube used influence success rates. 1.3 Methods A retrospective chart analysis of all patients - independent of the underlying pathology - undergoing surgery of the lacrimal drainage system between 1st of January 2013 and 31st December 2017. Success rates and patient profiles will be analyzed not only for all patients, but also for subgroups based on the underlying pathology and operation performed.

NCT ID: NCT04930809 Completed - Healthy Clinical Trials

Single and Multiple Dose Study of VER-01 in Healthy Volunteers

Start date: November 25, 2021
Phase: Phase 1
Study type: Interventional

Evaluation of pharmacokinetics, tolerability and safety of VER-01 in healthy volunteers

NCT ID: NCT04930796 Completed - Healthy Clinical Trials

Food Effect Study of VER-01 in Healthy Volunteers

Start date: August 10, 2022
Phase: Phase 1
Study type: Interventional

Evaluation of pharmacokinetics, tolerability and safety of VER-01 depending on the intake a high-fat meal in healthy volunteers

NCT ID: NCT04927325 Completed - Digital Technology Clinical Trials

Erythema at Exit Site & Tablet Camera

Start date: June 30, 2021
Phase: N/A
Study type: Interventional

Background: In critical care medicine central venous catheters play an important role in the source of infections. In the daily routine prior to the diagnosis the suspicion of catheter related infection is discussed in the medical team due to signs of systemic inflammation or exit site infection like erythema, induration or tenderness. However, if an erythema at exit site of a central line can be quantified with a tablet camera, is unknown. Methods: Standardized set of photos will be taken of 10 central lines with a reddened exit site and 10 catheters without an erythema (as a control over time) with a tablet camera and a single-lens reflex camera. The percentage of usable images between tablet and single-lens reflex camera will be analysed. Furthermore, two independent clinical experts from dermatology will grade blinded de-identied images on a scale from 0 to 4 (0 - no erythema, 1- very faint, 2 - faint, 3 - bright, 4 - very bright). Objectives: The primary objective of this feasibility study aims to analyze the reliability of a tablet camera as a device for quantification of erythema around an exit site.

NCT ID: NCT04924972 Completed - Clinical trials for Dermatochalasis of Upper Eyelid

FACE-Q in Blepharoplasty

Start date: February 1, 2019
Phase:
Study type: Observational

The aim of this study is to assess the effect of two different suturing techniques in patients undergoing bilateral upper eyelid blepharoplasty on the results of the FACE-Q Eye Module questionnaire for measuring patient-reported outcomes as well as on the blinded objective assessment by two experienced surgeons using the same questionnaire. We aim to investigate the differences of the 2 most common techniques of skin closure with running cutaneous or subcuticular Nylon (6-0 Prolene) sutures in upper blepharoplasties and their effect on postoperative complications and scar formation. Besides the functional outcomes (visual field) and objective postoperative results, we aim to measure the patients' satisfaction using the FACE-Q Eye Module as a comprehensive, procedure- and disease-specific patient-reported outcome instrument.

NCT ID: NCT04918888 Completed - Covid19 Clinical Trials

COVID-19 Vaccination in Oncologic Patients

VINCI
Start date: April 19, 2021
Phase:
Study type: Observational

Evaluating the vaccination willingness in oncologic patients over six months as well as estimating the effects of radiotherapy/systemic anticancer treatment on the efficacy and toxicity of currently approved SARS-CoV-2 vaccines

NCT ID: NCT04917588 Completed - Abnormal Lip Clinical Trials

Study to Evaluate the Effectiveness, Safety and Long Term Safety of Saypha® FILLER Lidocaine for Lip Augmentation

SayLip
Start date: July 28, 2020
Phase: Phase 3
Study type: Interventional

This is a prospective, open-label, multicentre, randomized study conducted to evaluate the effectiveness, safety and long-term safety of Saypha® FILLER Lidocaine for lip augmentation.

NCT ID: NCT04917081 Completed - Meditation Clinical Trials

'Go With the Flow': Effects of Mindful Self-Compassion in Psychiatric Rehabilitation

Start date: September 11, 2020
Phase: N/A
Study type: Interventional

This study is designed as a randomized controlled trial to gain further insights into possible effects of a standardized 6-week Mindful Self-Compassion (MSC) training on psychiatric rehabilitation inpatients and aims - to generate insights into which parameters of mental health, and especially emotion regulation, can be improved by MSC in this setting, - to compare effects of MSC training with an established relaxation training (i.e., progressive muscle relaxation; PMR) and - to determine the general conditions and patient characteristics influencing the effectiveness of MSC training.

NCT ID: NCT04916665 Completed - Clinical trials for Short Bowel Syndrome

Bridging Intestinal Failure With Teduglutide - a Case Report

Start date: January 1, 2019
Phase:
Study type: Observational

In this case report the investigators present a novel strategy for using teduglutide as a bridging therapy to intestinal reconstruction.