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NCT ID: NCT02199262 Completed - Agitation Clinical Trials

Quality Improving Program on Agitation in the Surgical Intensive Care Unit

Start date: February 2004
Phase: N/A
Study type: Interventional

Agitation in the intensive care unit can have multiple consequences. The investigators hypothesize that agitation and its consequences can be reduced by the introduction of a reminder aiming at guiding the management of agitation. The investigators also hypothesize that they can prevent agitation and its consequences by acting on patients environment with reafferentation and relaxation methods. The investigators' objectives are to test within a quality improvement project by a prospective randomized study: - If by reducing the number of agitation episodes we reduce the number of harmful consequences. - If the introduction of reafferentation and relaxation methods (music therapy or reflexology) can prevent the occurrence of agitation. - If the introduction of a reminder on management of agitation can reduce the number of agitation episodes. This study is conducted in an18 general surgical ICU beds receiving 1600 patients / year for a total of 6900 hospital /days /year, in a tertiary teaching hospital. The study is organized in 3 phases: 1. First phase: Baseline phase (Prospective analysis of the present situation) 2. Second phase: Learning phase (Implementation of a reminder about the management of agitation and delirium ) 3. Third phase: Randomized Intervention (reminder alone vs addition of music or reflexology) The interventions are : 1. Implementation of a reminder of guidelines of agitation diagnosis and management. 2. Music intervention( see description below) + reminder 3. Reflexology (see description below)+ reminder Agitation is monitored with two scales SAS and CAM-ICU(description below) . Harmful consequences and complications are systematically registered as well as medication and the use of contention methods. Adherence to the implemented monitoring and interventions is also regularly checked. Data are daily collected (see details below) Statistical analysis and power calculation (see below)

NCT ID: NCT02198937 Terminated - Inflammation Clinical Trials

Investigation on the Effect of Smoking on the Expression of Pro- and Anti-thrombotic, Anti-oxidative, and Inflammatory Markers in Humans

Start date: June 2014
Phase: N/A
Study type: Observational

Investigation on the effect of smoking on thrombus formation in humans. The expression of pro- and anti-thrombotic, anti-oxidative, and inflammatory markers will be assessed in 25-50 year old healthy smokers and non-smokers. The investigators are interested in possible differences between the two groups.

NCT ID: NCT02198599 Completed - Stroke Clinical Trials

Mobility Enhancing Nursing Intervention

MFP
Start date: March 2011
Phase: N/A
Study type: Interventional

Objectives: This parallel RCT investigated the effect of a new nursing intervention (Mobility Enhancing Nursing Intervention - MFP) designed to improve the rehabilitation programs' outcomes and patients' quality of life. Intervention: The IG combined standard care with the 30-day mobility-enhancing-nursing intervention (MFP). MFP placed patients on a mattress on the floor and used constant tactile-kinaesthetic stimulation in everyday tasks to increase spatial orientation, to teach patients to get up safely and to move independently. Primary and secondary outcome measures: Outcomes were defined as functionality (Extended Barthel Index, EBI), quality of life (WHOQoL), and fall-related self-efficacy (FES-I).

NCT ID: NCT02198391 Completed - Clinical trials for Respiratory Tract Diseases

Study of Echinaforce Junior Tablets in Children With Acute Colds

Start date: October 15, 2014
Phase:
Study type: Observational

This study aims to investigate safety and efficacy of Echinaforce Junior tablets in two dosages of 3 x 1 and 5 x 1 tablets per day in children 4 - 12 years old with acute colds.

NCT ID: NCT02197416 Completed - Clinical trials for Venous Thromboembolism

Safety of Dabigatran Etexilate in Blood Clot Prevention in Children

Start date: September 29, 2014
Phase: Phase 3
Study type: Interventional

This open-label, single arm prospective cohort study will assess the safety of dabigatran etexilate in secondary prevention of venous thromboembolism in paediatric patients. Children from 0 to less than 18 years of age will be eligible to participate.

NCT ID: NCT02197260 Completed - Clinical trials for Chronic Periodontitis

Antimicrobial Therapy as Adjunct to Periodontal Treatment: Effect of Timing

GAR
Start date: September 2008
Phase: Phase 4
Study type: Interventional

It is common practice to carry out the therapy of periodontal diseases in two phases. In a first, non-surgical phase, bacterial deposits on tooth surfaces (plaque and calculus) are removed using a cleaning method called "scaling and root planing" (SRP). After three to six months the case is evaluated and, if necessary, further treatment is provided, usually taking a more aggressive, surgical approach. Beneficial effects of adjunctive systemic antibiotics on clinical outcomes have been shown repeatedly but specific indications for antibiotics in subgroups of diseased patients, and the optimal timing of antimicrobial therapy, continue to be issues of a long lasting controversy.This study assessed the differential outcomes of periodontal therapy supplemented with amoxicillin-metronidazole during either the non-surgical or the surgical treatment phase.

NCT ID: NCT02196428 Completed - Telemedicine Clinical Trials

Medical Telemonitoring Plus Individual Teleconsultation in Elderly

Start date: September 2014
Phase: N/A
Study type: Interventional

The aim of this study is to explore the requirements and conditions of medical teleconsultation and remote diagnostics (telemonitoring) of older people in the residential environment with an emphasis on the need for adaptation, feasibility and acceptance of telemedicine services to a web based documentation and communication platform (Ambient Assisted Living Wizard).

NCT ID: NCT02196415 Completed - Clinical trials for Congenital Medial Deviation

Three-Dimensional Hindfoot Alignment Measurements Based On Biplanar Radiographs: Prospective Clinical Feasibility Study

Start date: July 2014
Phase:
Study type: Observational

- The measurement of hindfoot alignment is a technical challenge. - Today, hindfoot alignment is typically measured on hindfoot alignment view radiographs or long axial view radiographs. Measurements on both types of radiographs are hampered by technical shortcomings such as minimal rotational misplacement of the foot at the time of image acquisition. In previous publications our study groups demonstrated substantial measurement errors due to these shortcomings as well as bad interreader agreement. - Hindfoot alignment measurement is feasible on MR images but hampered by the non-weight-bearing position of the patient and therefore not suited for pre-treatment evaluation. - In an ex vivo study using plastic phantoms of a foot our research group could demonstrate superior interreader agreement and complete correction for foot misplacement at the time of image acquisition using a 3D secondary measurement technique based on biplanar low dose radiographs. - Image acquisition using biplanar low dose radiographs is associated with a substantial reduction (about 1/7) of radiation dose applied to the patient compared to standard radiographs. - Therefore the question arises if these excellent ex vivo results can be confirmed in a prospective clinical study. Objectives: 1. Evaluation of technical feasibility of 3D hindfoot alignment measurements based on biplanar radiographs. 2. Reproduction of superior interreader agreement of measurements based on biplanar radiographs compared to measurements on conventional radiographs.

NCT ID: NCT02196337 Completed - Iodine Deficiency Clinical Trials

Salt Iodization: Meeting the Needs of Pregnancy, Lactation and Infancy

SIMPLIFY
Start date: July 2014
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether universal salt iodization (USI) meets the iodine requirements of pregnant women, lactating women and infants.

NCT ID: NCT02196155 Recruiting - Plantar Fasciitis Clinical Trials

Botulinum Toxin A Versus Steroids for the Treatment of Chronic Plantar Fasciitis

Start date: July 2016
Phase: N/A
Study type: Interventional

Plantar fasciitis is the classic and most common type of heel pain. Considering the costs for health care and the temporary disability not only for work, plantar fasciitis results in a substantial (and at least partially unnecessary) burden for the Swiss health care system and national economics. Nonoperative treatment is the mainstay of treating plantar fasciitis. However, so far no treatment has proven to be superior to others, and there is national and international lack of consensus of how to treat plantar fasciitis best. The investigators believe that the BTX-A injection in the gastrocnemius and the soleus muscles is currently the most promising non-operative approach, because it is considered to treat the disease at its origin (temporary weakening of the tight triceps surae muscle) as opposed to simply alleviate the symptoms (e.g. plantar cortisone and other injections, ESWT). However, to date there is no evidence in the literature that compares the new, promising technique of BTX-A injection into the gastroc-soleus complex to a sham (saline) injection and to the gold standard steroid injection at the plantar fascia insertion site. With the intended study, this gap is going to be closed.