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NCT ID: NCT02809131 Completed - Syncope Clinical Trials

Perioperative Antibiotic Therapy to Prevent Cardiac Implantable Electronic Device Infections.

ENVELOPE
Start date: April 1, 2016
Phase: Phase 3
Study type: Interventional

The number of cardiac implantable electronic devices (CIEDs) implanted each year has grown rapidly over the past two decades. CIED infections, defined as infections involving the generator implant site (pocket) and/or intravascular leads, have become increasingly prevalent, with the rate of growth in infections outpacing that of CIED procedures. The odds of both short term and long term mortality are at least doubled in patients who suffer CIED infections, and long term survival is particularly poor in women. Optimal strategies to prevent CIED infections in high-risk patients are largely unproven. However, recent observational studies of an antibiotic-coated envelope implanted at the time of CIED procedure have shown that this strategy is associated with a low incidence of CIED infections. Other interventions to prevent CIED infections, including the use of antibiotic irrigant used to wash the pocket during implantation and postoperative oral antibiotics, are commonly used but not supported by rigorous controlled studies. The Specific Aim of this study is to test the hypothesis that the use of the antibacterial envelope alone is noninferior to a strategy using the antibacterial envelope and intraoperative antibacterial irrigant and postoperative oral antibiotics for the reduction of cardiac implantable device infections in patients with ≥2 risk factors for infection.

NCT ID: NCT02814929 Completed - Clinical trials for Retinopathy of Prematurity

Incidence, Risk Factors and Severity of Retinopathy of Prematurity (ROP) in Turkey

TR-ROP
Start date: April 1, 2016
Phase:
Study type: Observational

The study includes preterm infants who are being screened for ROP between April 1,2016 and April 30, 2017 in 69 neonatal intensive care units (NICUs) in Turkey. Infants with birth weight (BW) of ≤1500 g or ≤32 weeks' gestation and those with a BW of greater than 1500 g or gestational age (GA) >32 weeks with an unstable clinical course are included. The incidence of any ROP, severe ROP and treatment modalities will be determined. The risk factors for ROP development will also be evaluated.

NCT ID: NCT02815150 Completed - Gastric Cancer Clinical Trials

Safety of 250ml Preoperative Carbohydrate Drink in Gastric Cancer Patients

Start date: April 1, 2016
Phase: N/A
Study type: Interventional

This study aims to assess the impact of preoperative oral carbohydrate drink on gastric emptying and PH of gastric fluid in gastric cancer patients directly. Furthermore, investigators aim to evaluate the safety and effectiveness of preoperative oral carbohydrate in elective gastric cancer surgery, providing direct evidence for clinical practice.

NCT ID: NCT02839993 Completed - Clinical trials for Healthy Older Adults

tDCS Effects on Associative Learning in Older Adults of Retirement Age

TRAINSTIM2
Start date: April 1, 2016
Phase: N/A
Study type: Interventional

The aim of this study is to investigate whether a tDCS-accompanied training of audio-visual associative memory leads to a performance improvement in healthy older individuals.

NCT ID: NCT02847793 Completed - Depression Clinical Trials

Attentional Bias Modification Through Eye-tracker Methodology (ABMET)

ABMET
Start date: April 1, 2016
Phase: N/A
Study type: Interventional

Cognitive biases are a hallmark of depression but there is scarce research on whether these biases can be directly modified by using specific cognitive training techniques. The aim of this study will be targeting and modifying specifically relevant attention biases in participants with subclinical depression using eye-tracking methodologies. This innovative approach has been proposed as a promising future line of intervention in Attention Bias Modification procedures (Koster & Hoorelbeke, 2015). Recent findings suggest that depression is characterized by a double attentional bias (Duque & Vazquez, 2015), More specifically, depressed individuals have difficulties both to disengage from negative materials (e.g., sad faces) and to engage with positive materials (e.g., happy faces). Thus, training procedures to change attentional biases should target these two separate components.

NCT ID: NCT02868931 Completed - Diabetes Mellitus Clinical Trials

Evaluation of a Diabetes Treatment and Education Program for Insulin Pump Therapy (INPUT)

INPUT
Start date: April 1, 2016
Phase: N/A
Study type: Interventional

This study is a randomized, controlled, prospective trial with a 6-month follow-up. A newly developed treatment and education programme for diabetic patients with an insulin pump therapy (INPUT) will be tested compared to a waiting group. Primary outcome variable is the difference in glycemic control between baseline and the 6-month follow-up. Secondary outcome variables are: severe hypoglycaemia, diabetes-related distress, depressive symptoms, health-related quality of life, diabetes empowerment, self-care behavior, hypoglycemia awareness, and attitudes towards insulin pump therapy.

NCT ID: NCT02899273 Completed - Dental Caries Clinical Trials

Perception of Children With Visible Untreated and Treated Caries

ECC-ET
Start date: April 1, 2016
Phase:
Study type: Observational [Patient Registry]

In Germany about 5 to 20% of children suffer from early childhood caries (ECC). Preceding results of eye-tracking-studies on the perception of patients with unilateral cleft and patients with severe orthognathic malocclusion let us assume that caries and missing teeth might influence the observer's focus. The aim of this study is to test the hypothesis that the faces of patients with ECC and patients with signs of dental treatment (crown, gap etc.) are contemplated differently from and assessed more negatively than healthy patients. Particular attention should be paid to potential differences between the findings of the two observer-groups (medical laypersons/ dental students).

NCT ID: NCT02952625 Completed - Clinical trials for Head and Neck Cancer

PET/MR in Radiotherapy for Head and Neck Cancer Pilot

Start date: April 1, 2016
Phase: N/A
Study type: Interventional

This is a pilot non-intervention study that aims to introduce PET/MRI, a state of the art new imaging technique, into the radiotherapy treatment pathway of patients with head and neck cancer. Ultimately the investigators aim to establish appropriate scanning and image registration protocols, to allow progression to a randomized trial of adaptive radiotherapy dose escalation. The latter is thought to potentially improve outcomes in this group. Ten patients with squamous cell carcinoma (SCC) of the oropharynx, hypopharynx and larynx, planned for radical treatment with radiotherapy (+/-chemotherapy), will be recruited. Study participants will have two PET/MRI scans, with the radiotherapy immobilization devices in situ. The first will be done prior to the start of radiotherapy, the second half way through treatment. Image quality will be assessed by comparing to standard diagnostic scans and different registration methods will be compared to establish the best way of incorporating PET/MR image data into the radiotherapy planning system. Patient tolerability and workflow considerations will also be qualitatively assessed. Furthermore, a planning study will be conducted to establish relevant treatment protocols for a subsequent dose escalation trial. PET/MRI is an exciting new technology with a lot of potential in the context of adaptive radiotherapy dose escalation. Within this pilot study the investigators aim to address the technical challenges of using it in this context prior to proceeding to a randomized trial.

NCT ID: NCT02955706 Completed - Alzheimer Disease Clinical Trials

Assessment the Efficacy of Acetyl-L-carnitine in Patient With Alzheimer's Disease

Start date: April 1, 2016
Phase: Phase 4
Study type: Interventional

clinical trial to assess the efficacy of Acetyl-L-carnitine

NCT ID: NCT02973568 Completed - Pain Clinical Trials

Comparative Study on Acute Pain Evaluation Between Spanish and French Hospital Emergency Unit

DASAU
Start date: April 1, 2016
Phase: N/A
Study type: Observational

Today, pain is a difficult affordable subject in Spain. There are however 187 units of pain care with a consultations rate in emergency center of more than 60%.For example OXYCODONE(opioid analgesic)is widely used while it's under used in Spain. In the same way MEOPA(Kalinox) is a new approach of pain care daily used as well in France (for example in dislocated shoulder pain, or ulceration care...etc) There are lots of studies relative to chronic pain but not too much about acute pain in Spain.That's why we want to focus our study on evaluation of acute pain treatment and efficacy in french and spanish hospital