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NCT ID: NCT04299165 Completed - Clinical trials for Pulmonary Disease, Chronic Obstructive

Smartphone-App as Maintenance Program in COPD

AMOPUR
Start date: August 9, 2019
Phase: N/A
Study type: Interventional

Increasing Physical activity (PA) is considered to be an important factor in an efficient management of the chronic obstructive pulmonary disease (COPD). The successful methods required to achieve improvements in PA following Pulmonary Rehabilitation (PR), however are sparsely reported. Therefore, the investigators conduct this trial to evaluate the effectiveness of using a COPD management program delivered to the patient through a mobile medical application Kaia COPD-App, after the completion of a PR.

NCT ID: NCT04298853 Completed - Clinical trials for Neonatal Abstinence Syndrome

Optimal Morphine Dosing Schedule for Neonatal Abstinence Syndrome

Start date: June 30, 2020
Phase: Phase 4
Study type: Interventional

Randomized pilot trial comparing scheduled morphine dosing with a weaning protocol to intermittent morphine dosing on an as-needed basis for newborns with neonatal abstinence syndrome.

NCT ID: NCT04298463 Completed - Clinical trials for Acute Bacterial Skin and Skin Structure Infection

Retrospective Effectiveness Study of Dalbavancin and Other Standard of Care of the Same Class in Patients With ABSSSI

REDS
Start date: June 18, 2020
Phase:
Study type: Observational

The aim of this study is to collect the data on the effectiveness of dalbavancin in terms of save of hospitalization days on patients treated between June 2017 and June 2019 in two countries (Italy and Greece) vs the other Standards of care of the same class (SoC; i.v. lipo and glycopeptides) in a real-life context. Time to discharge from the start of therapy for ABSSSI in the hospital context will be assessed and all relevant data available on patient management, clinical, microbiological and safety outcomes during hospitalization and in the follow-up visits up to 30 days from discharge will be collected and evaluated.

NCT ID: NCT04298346 Completed - Premature Clinical Trials

Neurological Fate, Prematurity and Genetic Susceptibility Factors

GENIMOC
Start date: March 9, 2020
Phase:
Study type: Observational

This study could help identify aggravating or protective genetic polymorphisms associated with cerebral palsy. Populations of premature babies at different risk of cerebral palsy could thus be individualized with an impact on their monitoring and on the pathophysiological understanding of the processes leading to neurological lesions.

NCT ID: NCT04298268 Completed - Clinical trials for Nephrectomy or Partial Nephrectomy With Parenchyma Removal

The CUSA Clarity Soft Tissue Removal Study

Start date: March 30, 2020
Phase:
Study type: Observational

To investigate the clinical performance and surgeon preferences of the CUSA® Clarity Ultrasonic Surgical Aspirator System for soft tissue removal during surgical procedures. This will be evaluated through the effectiveness of soft tissue removal per surgeon assessment and Incidence of Adverse Device Effects.

NCT ID: NCT04297956 Completed - Clinical trials for Puerperal Depression

Survey on Patients After Childbearth Following Bariatric Surgery

SPOtMom
Start date: February 5, 2020
Phase:
Study type: Observational

Women with a history of bariatric surgery may face various difficulties during pregnancy and puerperal time. Therefore it is assumed the prevalence of mental health disorders might be higher than in average women during and after pregnancy. This could possibly lead to an unsatisfying weight progress and therapeutic non-adherence. These factors shall be observed in the study in order to characterize this special cohort of participants.

NCT ID: NCT04297579 Completed - Clinical trials for Congenital Melanocytar Nevi in the Lower Limb

Congenital Naevi of Lower Limb in the Child

NAEVUS
Start date: January 1, 1984
Phase:
Study type: Observational

Depending on its dimensions, it is difficult to predict if a congenital nevi of the lower limb can be surgically removed by a unique simple procedure or by a complex procedure (expander, skin graft etc..), with a good result. This study retrospectively reviewed the practice of our team of surgeons depending on the size of the naevus to reveal a dimension threshold that can be used in the future to help to choose between a simple or a complex procedure.

NCT ID: NCT04297397 Completed - Clinical trials for Respiratory Insufficiency

Personalised Simulation Technologies for Optimising Treatment in the Intensive Care Unit

PSTOTICU
Start date: February 20, 2020
Phase:
Study type: Observational

This project aims to develop software models describing how critically ill patients respond to changes in their treatment whilst admitted to an Intensive Care Unit (ICU). We will use high performance computers to fit software models to the physiological and treatment data of patients receiving mechanical ventilation.

NCT ID: NCT04297384 Completed - Breast Carcinoma Clinical Trials

Breast Cancer Pathways Program Impact on Patient Shared Decision Making and Experience in Academic and Community Practice

Start date: February 6, 2019
Phase: N/A
Study type: Interventional

This trial studies the impact of the breast cancer pathways program on the patient experience, including decision making and quality of life. Measuring how the breast cancer pathways program affects decision making and quality of life in patients may help doctors improve cancer education.

NCT ID: NCT04296968 Completed - Clinical trials for Experimental Pain in Healthy Human Participants

Sensory Evidence and Expectations in Pain Processing

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

Pain is a highly complex and subjective phenomenon which is not only rooted in sensory information but also shaped by cognitive processes such as expectation. However, the interaction of brain activity cording sensory information and expectation in pain processing are not completely understood. Predictive coding models postulate specific hypothesis about the interplay between bottom-up sensory information and top-down expectations in terms of prediction errors and predictions, respectively. They further implicate brain oscillations at different frequencies, which play a crucial role in processing prediction errors and predictions. More specifically, recent evidence in visual and auditory modalities suggests that predictions are reflected by alpha (8-13 Hz) and beta oscillations (14-30 Hz) and prediction errors by gamma oscillations (60-100 Hz). However, for the processing of pain, these frequency-specific relationships have not been addressed so far. The current project aims to investigate brain activity which reflects predictions, prediction errors and sensory evidence in pain processing using a cueing paradigm. To this end, we will apply painful stimuli with low and high intensity to the dorsum of the left hand in 50 healthy subjects. A visual cue, preceding to each painful stimulus, will predict the intensity of the consecutive painful stimulus (low vs. high) with a probability of 75%. After each painful stimulus, participants will be asked to rate the perceived pain intensity. Electroencephalography (EEG) and skin conductance will be recorded continuously during anticipation and stimulation intervals. This paradigm enables us to compare pain-associated brain responses of validly and invalidly cued trials, i.e. the representation of the prediction error, on the one hand. On the other hand, brain activity related to predictions can be investigated in the anticipation interval preceding to the painful stimulus by comparing trials with low and high intensity cues. Further, we will compare models including predictions, prediction error and sensory evidence to ascertain the involvement of each brain response in processing sensory information and expectation. Results of the study promise to elucidate the interplay of predictions, predictions errors and sensory evidence in pain processing and how they differentially relate to neural oscillations at different frequency bands and pain-evoked responses.